FDA Inspection 1280532 — Midwest Products And Engineering, Inc.

Midwest Products And Engineering, Inc. — FEI 3003500271

The FDA completed an inspection of Midwest Products And Engineering, Inc. on Aug 29, 2025 in Milwaukee, WI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 29, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Milwaukee, WI (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures

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