# FDA Inspection 756269 - Zimmer Biomet Mid Atlantic - November 29, 2011

Source: https://www.keypedia.com/records/fda_inspections/zimmer-biomet-mid-atlantic/1f9ee39c-57d1-431a-bdbb-27332a03c1bd
Source feed: FDA_Inspections

> FDA Inspection 756269 for Zimmer Biomet Mid Atlantic on November 29, 2011. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 756269
- Company Name: Zimmer Biomet Mid Atlantic
- Inspection Date: 2011-11-29
- Classification: No Action Indicated (NAI)
- Project Area: Human Cellular, Tissue, and Gene Therapies
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

## Related Documents

- [FDA Inspection 596505 - 2009-07-14](https://www.keypedia.com/records/fda_inspections/zimmer-biomet-mid-atlantic/79aea3f9-ee1c-4ce9-bb3f-13836b4cc9d3)

Company: https://www.keypedia.com/companies/zimmer-biomet-mid-atlantic/1cd1bb42-1242-4419-8505-3b1110a79207

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