FDA Inspection 565562 — Zimmer Manufacturing B.V.
The FDA completed an inspection of Zimmer Manufacturing B.V. on February 27, 2009 in Mercedita, PR. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- February 27, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Bioresearch Monitoring
- Location
- Mercedita, PR (United States)
Additional Details
Postmarket Audit Inspections