FDA Inspection 819321 — FIS - Fabbrica Italiana Sintetici SpA
The FDA completed an inspection of FIS - Fabbrica Italiana Sintetici SpA on Feb 7, 2013 in Lonigo. 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
- Feb 7, 2013
- Fiscal Year
- 2013
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Lonigo (Italy)