FDA Inspection 990211 — Laboratoires Anios

Laboratoires Anios — FEI 3004094142

The FDA completed an inspection of Laboratoires Anios on May 27, 2016 in Sainghin-En-Melantois. 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
May 27, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sainghin-En-Melantois (France)

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