FDA Inspection 989581 — BioReliance Limited
The FDA completed an inspection of BioReliance Limited on Sep 7, 2016 in Penicuik. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Sep 7, 2016
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Penicuik (United Kingdom)