FDA Inspection 1009629 — Hartmut Doehner, M.D.

Hartmut Doehner, M.D. — FEI 3012812077

The FDA completed an inspection of Hartmut Doehner, M.D. on Jan 20, 2017 in Ulm. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 20, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Ulm (Germany)

Additional Details

Clinical Investigator (CI)

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