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