# FDA Inspection 1280532 - Midwest Products and Engineering Inc - August 29, 2025

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

> FDA Inspection 1280532 for Midwest Products and Engineering Inc on August 29, 2025. Classification: No Action Indicated (NAI).

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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)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Minneapolis District Office

## Related Documents

- [FDA Inspection 1280532 - 2025-08-29](https://www.globalkeysolutions.net/records/fda_inspections/midwest-products-and-engineering-inc/048bdb0f-a8b7-4480-a79c-4d343f56e129)
- [FDA Inspection 1280532 - 2025-08-29](https://www.globalkeysolutions.net/records/fda_inspections/midwest-products-and-engineering-inc/a5b85398-fbfc-4dfc-b2d3-d0509fdb7379)
- [FDA Inspection 1280532 - 2025-08-29](https://www.globalkeysolutions.net/records/fda_inspections/midwest-products-and-engineering-inc/36e32fb3-0cf8-4132-8c86-6a3d69cd5277)
- [FDA Inspection 1203163 - 2023-04-21](https://www.globalkeysolutions.net/records/fda_inspections/midwest-products-and-engineering-inc/c954fc29-f388-4da7-81f5-2af18be6b81b)
- [FDA Inspection 1203163 - 2023-04-21](https://www.globalkeysolutions.net/records/fda_inspections/midwest-products-and-engineering-inc/39e31a9a-022e-4b01-99fa-0c9307572649)

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

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