FDA Inspection 1097949 — FUJIFILM Diosynth Biotechnologies UK Limited
The FDA completed an inspection of FUJIFILM Diosynth Biotechnologies UK Limited on Nov 16, 2018 in Billingham. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Nov 16, 2018
- Fiscal Year
- 2019
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Billingham (United Kingdom)
Additional details
Mutual Recognition Agreement (MRA)