FDA Inspection 1015858 — Gustavo Frechtel

Gustavo Frechtel — FEI 3013325951

The FDA completed an inspection of Gustavo Frechtel on June 2, 2017 in Caba, Na C1419ahn. 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 2, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Caba, Na C1419ahn (Argentina)

Additional Details

Clinical Investigator (CI)