FDA Inspection 971540 — Micronisierungs-Kontor Oberrot GmbH

Micronisierungs-Kontor Oberrot GmbH — FEI 3005909896

The FDA completed an inspection of Micronisierungs-Kontor Oberrot GmbH on Mar 17, 2016 in Oberrot. 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 17, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Oberrot (Germany)

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