FDA Inspection 559762 — FUJIFILM Diosynth Biotechnologies UK Limited
The FDA completed an inspection of FUJIFILM Diosynth Biotechnologies UK Limited on January 9, 2009 in Billingham. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- January 9, 2009
- Fiscal Year
- 2009
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Billingham (United Kingdom)