FDA Inspection 1008030 — Jose Fernando Molina Restrepo, M.D.

Jose Fernando Molina Restrepo, M.D. — FEI 3012819915

The FDA completed an inspection of Jose Fernando Molina Restrepo, M.D. on Dec 9, 2016 in Medellin. 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). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 9, 2016
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Medellin (Colombia)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
756021 CFR 312.60FD-1572, protocol compliance

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