# Midwest Products and Engineering Inc – FDA Inspection, Aug 29, 2025

Source: https://www.keypedia.com/records/fda_inspections/midwest-products-and-engineering-inc/74bb8f92-2339-4dc3-a86e-e892a586bf9d
Source feed: FDA_Inspections

> FDA inspection 1280532 of Midwest Products and Engineering Inc, August 29, 2025. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1280532
- Company Name: Midwest Products and Engineering Inc
- Inspection Date: 2025-08-29
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Minneapolis District Office
- Citation Count: 2

## Related Documents

- [FDA Inspection 1203163 - 2023-04-21](https://www.keypedia.com/records/fda_inspections/midwest-products-and-engineering-inc/c954fc29-f388-4da7-81f5-2af18be6b81b)

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/chad-e-schmear/275a4c57-d288-46f9-8257-64fcd96159ce)

Company: https://www.keypedia.com/companies/midwest-products-and-engineering-inc/8a6fa11e-fc45-4e1e-a6bd-1f524752d635

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d