FDA Inspection 608009 — KEDPlasma, LLC
The FDA completed an inspection of KEDPlasma, LLC on Aug 26, 2009 in Pensacola, 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
- Aug 26, 2009
- Fiscal Year
- 2009
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Pensacola, FL (United States)