FDA Inspection 1098174 — Karl Mann, M.D.

Karl Mann, M.D. — FEI 3015266336

The FDA completed an inspection of Karl Mann, M.D. on June 28, 2019 in Mannheim. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 28, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Mannheim (Germany)

Additional Details

Clinical Investigator (CI)