FDA Inspection 1107515 — Anidro Do Brasil Extracoes S.A.

Anidro Do Brasil Extracoes S.A. — FEI 3002807563

The FDA completed an inspection of Anidro Do Brasil Extracoes S.A. on Oct 25, 2019 in Parnaiba. 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
Oct 25, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Parnaiba (Brazil)

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