FDA Inspection 594572 — Bioreliance Ltd.
The FDA completed an inspection of Bioreliance Ltd. on July 1, 2009 in Stirling, Scotland. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- July 1, 2009
- Fiscal Year
- 2009
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Stirling, Scotland (United Kingdom)