FDA Inspection 1088285 — Haupt Pharma Wuelfing GmbH

Haupt Pharma Wuelfing GmbH — FEI 3003183252

The FDA completed an inspection of Haupt Pharma Wuelfing GmbH on Dec 7, 2018 in Gronau (Leine). The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Veterinary.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Dec 7, 2018
Fiscal Year
2019
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Gronau (Leine) (Germany)

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