FDA Inspection 976630 — BioReliance Limited
The FDA completed an inspection of BioReliance Limited on Mar 17, 2016 in Penicuik. 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
- Mar 17, 2016
- Fiscal Year
- 2016
- Product Type
- Biologics
- Project Area
- Vaccines and Allergenic Products
- Location
- Penicuik (United Kingdom)