# FDA Inspection 632322 - Midwest Biomet Inc - December 02, 2009

Source: https://www.keypedia.com/records/fda_inspections/midwest-biomet-inc/02ec7a90-0ec0-4acf-8df6-f0603e596505
Source feed: FDA_Inspections

> FDA Inspection 632322 for Midwest Biomet Inc on December 02, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 632322
- Company Name: Midwest Biomet Inc
- Inspection Date: 2009-12-02
- Classification: No Action Indicated (NAI)
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

Company: https://www.keypedia.com/companies/midwest-biomet-inc/e31068ce-b7eb-4bb0-996a-623a78b03d47

Office: https://www.keypedia.com/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d