FDA Inspection 877801 — Haupt Pharma Wuelfing GmbH

Haupt Pharma Wuelfing GmbH — FEI 3003183252

The FDA completed an inspection of Haupt Pharma Wuelfing GmbH on March 28, 2014 in Gronau (Leine). The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 28, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Gronau (Leine) (Germany)

Citations

IDCFRDescription
110521 CFR 211.22(d)Procedures not in writing, fully followed
121321 CFR 211.67(a)Cleaning / Sanitizing / Maintenance