FDA Inspection 1110441 — Wacker Biotech GmbH

Wacker Biotech GmbH — FEI 3008840280

The FDA completed an inspection of Wacker Biotech GmbH on Sep 6, 2019 in Halle (Saale). 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
Sep 6, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Halle (Saale) (Germany)

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