FDA Inspection 1098174 — Karl Mann, M.D.

Karl Mann, M.D. — FEI 3015266336

The FDA completed an inspection of Karl Mann, M.D. on Jun 28, 2019 in Mannheim. 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
Jun 28, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Mannheim (Germany)

Additional details

Clinical Investigator (CI)

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