FDA Inspection 1123641 — FIS - Fabbrica Italiana Sintetici S.p.A
The FDA completed an inspection of FIS - Fabbrica Italiana Sintetici S.p.A on June 1, 2018 in Termoli. 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
- June 1, 2018
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Termoli (Italy)
Additional Details
Mutual Recognition Agreement (MRA)