FDA Inspection 1072361 — BPL Plasma Inc
The FDA completed an inspection of BPL Plasma Inc on Oct 30, 2018 in Queens Village, NY. 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
- Oct 30, 2018
- Fiscal Year
- 2019
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Queens Village, NY (United States)