FDA Inspection 571582 — Fersinsa GB, SA De CV

Fersinsa GB, SA De CV — FEI 3000538793

The FDA completed an inspection of Fersinsa GB, SA De CV on Jan 19, 2009 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
Jan 19, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ramos Arizpe (Mexico)

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