FDA Inspection 1080953 — Heinrich Klenk GmbH & CO KG

Heinrich Klenk GmbH & CO KG — FEI 3014716333

The FDA completed an inspection of Heinrich Klenk GmbH & CO KG on Dec 12, 2018 in Roethlein. 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
Dec 12, 2018
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Roethlein (Germany)

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