FDA Inspection
Midwest Products and Engineering IncMidwest Products and Engineering Inc – FDA Inspection, Aug 29, 2025
Record Details
This FDA Inspection record concerns Midwest Products and Engineering Inc, with an inspection on August 29, 2025, issued by the Minneapolis District Office, covering medical devices & rad health.
- Inspection Date
- August 29, 2025
- Product Type
- Medical Devices & Rad Health
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ID · 74bb8f92-2339-4dc3-a86e-e892a586bf9d
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1280532
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Medical Devices
FDA Citations
2- 21 CFR 820.100(a)Lack of or inadequate procedures
- 21 CFR 820.50Purchasing controls, Lack of or inadequate procedures
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Other FDA inspections of Midwest Products and Engineering Inc
1| Date | Classification | Office | Project area |
|---|---|---|---|
| April 21, 2023 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
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