FDA Inspection 1110441 — Wacker Biotech GmbH

Wacker Biotech GmbH — FEI 3008840280

The FDA completed an inspection of Wacker Biotech GmbH on September 6, 2019 in Halle (Saale). The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 6, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Halle (Saale) (Germany)