FDA Inspection 759166 — Aesica Pharmaceuticals GmbH

Aesica Pharmaceuticals GmbH — FEI 3002948883

The FDA completed an inspection of Aesica Pharmaceuticals GmbH on Nov 8, 2011 in Zwickau. 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
Nov 8, 2011
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Zwickau (Germany)

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