FDA Inspection 1127151 — Hevert Arzneimittel GmbH & Co. KG

Hevert Arzneimittel GmbH & Co. KG — FEI 3010165877

The FDA completed an inspection of Hevert Arzneimittel GmbH & Co. KG on Mar 12, 2020 in Nusbaum. 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
Mar 12, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Nusbaum (Germany)

Additional details

Mutual Recognition Agreement (MRA)

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