FDA Inspection 896701 — Fersinsa GB, SA de CV

Fersinsa GB, SA de CV — FEI 3000538793

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