FDA Inspection 1242874 — Brigiette Kalsch, M.D.

Brigiette Kalsch, M.D. — FEI 3006660278

The FDA completed an inspection of Brigiette Kalsch, M.D. on Jun 14, 2024 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 14, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Mannheim (Germany)

Additional Details

Clinical BA/BE