FDA Inspection 896701 — Fersinsa GB, SA De CV
The FDA completed an inspection of Fersinsa GB, SA De CV on Sep 10, 2014 in Ramos Arizpe. 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
- Sep 10, 2014
- Fiscal Year
- 2014
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Ramos Arizpe (Mexico)