FDA Inspection 548447 — Farmea

Farmea — FEI 3003583056

The FDA completed an inspection of Farmea on Oct 23, 2008 in Angers Cedex 01. 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
Oct 23, 2008
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Angers Cedex 01 (France)

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