# Midwest Products and Engineering Inc – FDA Inspection, Apr 21, 2023

Source: https://www.keypedia.com/records/fda_inspections/midwest-products-and-engineering-inc/c954fc29-f388-4da7-81f5-2af18be6b81b
Source feed: FDA_Inspections

> FDA inspection 1203163 of Midwest Products and Engineering Inc, April 21, 2023. Classification: Voluntary Action Indicated (VAI). 4 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: 1203163
- Company Name: Midwest Products and Engineering Inc
- Inspection Date: 2023-04-21
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- [FDA Inspection 1280532 - 2025-08-29](https://www.keypedia.com/records/fda_inspections/midwest-products-and-engineering-inc/74bb8f92-2339-4dc3-a86e-e892a586bf9d)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/amanda-dinaro/6df79979-ad5c-46f5-8917-197f8a0870e0)

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

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7