FDA Inspection 1134615 — Laila Arash-Kaps, M.D.

Laila Arash-Kaps, M.D. — FEI 3017298970

The FDA completed an inspection of Laila Arash-Kaps, M.D. on November 6, 2020 in Mainz. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 6, 2020
Fiscal Year
2021
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Mainz (Germany)

Additional Details

Clinical Investigator (CI)