FDA Inspection 1083280 — Lajos Kemeny, M.D.

Lajos Kemeny, M.D. — FEI 3015097867

The FDA completed an inspection of Lajos Kemeny, M.D. on Feb 22, 2019 in Szeged. 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
Feb 22, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Szeged (Hungary)

Additional Details

Clinical Investigator (CI)

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