Shiftmate
Production quality control records Excel template
Record the quantities of products checked and found non-conforming on a batch basis. Excel with non-compliance rate and user-defined threshold warning.
Prepared by:Shiftmate Product and Operations Team · Son kontrol:
Actual file previews
The images below are the actual data entry and executive summary pages of the workbook to be downloaded.


Step by step usage
Examine the example and prepare the blank file
One line is single batch control. If there are several defects in the same product, count the number of nonconforming products only once. The quantity checked is a sample, not the entire production quantity. Write the threshold rate as your internal tracking criterion; The file does not set a quality standard. Use the yellow input fields on the tracking page; Do not change the blue formula fields. The sample sheet is filled with fictitious records and does not count towards the actual work total.
Write actual records in the yellow fields
Appropriate quantity is the controlled minus improper quantity. Non-conformance rate is non-conformance/controlled. If the rate is greater than the threshold, it appears Threshold exceeded, if it is equal or less than it appears in Threshold. The overall ratio is the total non-compliant/total checked calculation, not the average of row percentages. The control amount cannot be zero; Inappropriate menstrual sample cannot be passed. An empty mandatory field is distinguished from a real zero. Correct missing or incorrect records in the control column; Since these lines are excluded from the summary, do not use the total as a final report until the problem is resolved.
Fix control alerts and review summary
Examine batches that exceed the threshold. Track error causes with separate action log.
What does this Excel file solve?
Record the quantities of products checked and found non-conforming on a batch basis. Excel with non-compliance rate and user-defined threshold warning. One line is single batch control. If there are several defects in the same product, count the number of nonconforming products only once. The quantity checked is a sample, not the entire production quantity. Write the threshold rate as your internal tracking criterion; The file does not set a quality standard. Use the yellow input fields on the tracking page; Do not change the blue formula fields. The sample sheet is filled with fictitious records and does not count towards the actual work total.
What's inside the file?
Suitable quantity, Inappropriate product rate, Threshold status. The file contains sample rows, canned formulas, data validation fields, risk colorings, and executive summary.
Calculation and control logic
Appropriate quantity is the controlled minus improper quantity. Non-conformance rate is non-conformance/controlled. If the rate is greater than the threshold, it appears Threshold exceeded, if it is equal or less than it appears in Threshold. The overall ratio is the total non-compliant/total checked calculation, not the average of row percentages. The control amount cannot be zero; Inappropriate menstrual sample cannot be passed. An empty mandatory field is distinguished from a real zero. Correct missing or incorrect records in the control column; Since these lines are excluded from the summary, do not use the total as a final report until the problem is resolved.
Worked example: Production quality control records: calculation example
200 items were checked. 8 non-conforming items. Internal tracking threshold is 3%. Result: 192 eligible products, 4% non-conformance and a Threshold exceeded warning occurs.
Decisions that can be taken as a result of this
Examine batches that exceed the threshold. Track error causes with separate action log
Common usage mistakes
Counting three defects in a single product as three inappropriate products. Mistaking the sample rate as the definitive result of the entire batch. Using the summary total as the final result without correcting the lines with control warnings
Limits and proper use
Acceptance sampling is not AQL, certification or product safety approval. Being within the threshold does not constitute authorization to ship. Follow your technical approval procedure separately. The file is prepared for 150 record lines. The parent summary includes all valid rows, regardless of filters. When capacity is full, open a new period copy; additional rows require the summary and validation ranges to be updated as well. There are no macros, external data connections or automatic notifications.
Compatibility and quality control
Two pages of this file were visually inspected; Formulas were recalculated and checked in empty, sample and incorrect entry scenarios. There was no separate device testing of the Excel desktop application. .xlsx without macro; formulas and drop-down lists are included in the file. The tracking page includes 150 preset record lines and a standalone Sample page. Prepared for desktop Excel; Check views and validations in other spreadsheet applications.
Scope of this file
This standalone file is intended for production quality control records. It's not that Shiftmate automates this industry workflow; The application focuses on team, shift and timesheet management.
Relevant official and technical resources
Frequently asked questions
Why isn't the overall rate the line average?
In order to weight samples of different sizes correctly, the total number of inappropriate items is divided by the total number of controls.
Does the threshold automatically come from the standard?
No. Your authorized team determines the threshold. There are no fixed sector or regulatory thresholds on file.
Would the entire batch be approved?
No. The result describes only the control sample entered. Party acceptance is a separate process.
Do I need to create an account to download the file?
No. You can download the Excel file directly after creating a download request with your email address. Creating a workspace is not mandatory. If there is an area that does not meet your needs, you can request an edit via the contact form.