FDA Inspection 920735 — Zimmer Etex
The FDA completed an inspection of Zimmer Etex on Apr 1, 2015 in Sanford, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Apr 1, 2015
- Fiscal Year
- 2015
- Product Type
- Biologics
- Project Area
- Human Cellular, Tissue, and Gene Therapies
- Location
- Sanford, FL (United States)