FDA Inspection 1218477 — MF Productions Saumur

MF Productions Saumur — FEI 3004713373

The FDA completed an inspection of MF Productions Saumur on Sep 15, 2023 in Bellevigne-Les-Chateaux. 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). 1 citation was issued during this inspection. Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 15, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bellevigne-Les-Chateaux (France)

Citations

IDCFRDescription
126321 CFR 211.68(b)Computer control of master formula records

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