# FDA Inspection 1310382 - Midwest-Tek, Inc. - April 01, 2026

Source: https://www.keypedia.com/records/fda_inspections/midwest-tek-inc/1677a577-c8ba-4269-8b67-1ce3e2b292d8
Source feed: FDA_Inspections

> FDA Inspection 1310382 for Midwest-Tek, Inc. on April 01, 2026. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1310382
- Company Name: Midwest-Tek, Inc.
- Inspection Date: 2026-04-01
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Office Name: Detroit District Office

## Related Documents

- [FDA Inspection 1310382 - 2026-04-01](https://www.keypedia.com/records/fda_inspections/midwest-tek-inc/fed62291-3630-476e-98ac-ffbadebda5d3)

Company: https://www.keypedia.com/companies/midwest-tek-inc/14df809a-c9fe-41fb-86cb-d51cb85a531d

Office: https://www.keypedia.com/offices/detroit-district-office/b09a1815-a000-40c0-bb44-5432ce87ed03