FDA Inspection 825841 — Hermes Arzneimittel GmbH

Hermes Arzneimittel GmbH — FEI 3001388094

The FDA completed an inspection of Hermes Arzneimittel GmbH on Feb 26, 2013 in Wolfratshausen. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Food/Cosmetics.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Feb 26, 2013
Fiscal Year
2013
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Wolfratshausen (Germany)

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