FDA Inspection 572942 — Coeur Inc.
The FDA completed an inspection of Coeur Inc. on April 1, 2009 in Washington, NC. 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
- April 1, 2009
- Fiscal Year
- 2009
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Washington, NC (United States)