FDA Inspection 598116 — Bioreliance Ltd.
The FDA completed an inspection of Bioreliance Ltd. on Jul 2, 2009 in Glasgow. 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
- Jul 2, 2009
- Fiscal Year
- 2009
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Glasgow (United Kingdom)