# Midwest Products and Engineering Inc, Milwaukee, WI – FDA Inspections

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

> Inspection records and compliance data for Midwest Products and Engineering Inc in Milwaukee, Wisconsin. 2 FDA inspections on record, 2 Form 483s, last inspected August 29, 2025.

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## Details

- Name: Midwest Products and Engineering Inc
- FEI Number: 3003500271
- Address Line 1: 10597 W Glenbrook Ct
- City: Milwaukee
- State: Wisconsin
- Zip Code: 53224
- Country Name: United States
- Address: 10597 W Glenbrook Ct, Milwaukee, Wisconsin 53224, United States
- Country: United States

## Related Documents

- [483 - Midwest Products and Engineering Inc - 2025-08-29](https://www.keypedia.com/records/483/midwest-products-and-engineering-inc/caf3d268-bfdd-43b8-9475-15944871b4ab) — source: FDA, date: August 29, 2025
- FDA Inspection 1280532 - Midwest Products and Engineering Inc - 2025-08-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 29, 2025
- [FDA Inspection 1280532 - Midwest Products and Engineering Inc - 2025-08-29](https://www.keypedia.com/records/fda_inspections/midwest-products-and-engineering-inc/74bb8f92-2339-4dc3-a86e-e892a586bf9d) — classification: No Action Indicated (NAI), source: FDA, date: August 29, 2025
- FDA Inspection 1280532 - Midwest Products and Engineering Inc - 2025-08-29 — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 29, 2025
- FDA Inspection 1280532 - Midwest Products and Engineering Inc - 2025-08-29 — classification: No Action Indicated (NAI), source: FDA, date: August 29, 2025
- [FDA Inspection 1203163 - Midwest Products and Engineering Inc - 2023-04-21](https://www.keypedia.com/records/fda_inspections/midwest-products-and-engineering-inc/c954fc29-f388-4da7-81f5-2af18be6b81b) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 21, 2023
- FDA Inspection 1203163 - Midwest Products and Engineering Inc - 2023-04-21 — classification: No Action Indicated (NAI), source: FDA, date: April 21, 2023

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