FDA Inspection 590672 — Arthomed, LLC.
The FDA completed an inspection of Arthomed, LLC. on Jun 19, 2009 in Delray Beach, 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
- Jun 19, 2009
- Fiscal Year
- 2009
- Product Type
- Biologics
- Project Area
- Human Cellular, Tissue, and Gene Therapies
- Location
- Delray Beach, FL (United States)