FDA Inspection 1054935 — BioLife Plasma Services L.P.
The FDA completed an inspection of BioLife Plasma Services L.P. on May 16, 2018 in Hayden, ID. 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
- May 16, 2018
- Fiscal Year
- 2018
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Hayden, ID (United States)