FDA Inspection 891979 — Valdepharm

Valdepharm — FEI 3000538143

The FDA completed an inspection of Valdepharm on Jul 10, 2014 in Val-De-Reuil. 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
Jul 10, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Val-De-Reuil (France)

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