FDA Inspection 1014956 — Fersinsa GB, SA De CV

Fersinsa GB, SA De CV — FEI 3000538793

The FDA completed an inspection of Fersinsa GB, SA De CV on Jun 13, 2017 in Ramos Arizpe. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jun 13, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ramos Arizpe (Mexico)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.