FDA Inspection 993015 — Kenia Castro, M.D.

Kenia Castro, M.D. — FEI 3012801633

The FDA completed an inspection of Kenia Castro, M.D. on Nov 3, 2016 in Hialeah, FL. 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). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 3, 2016
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Hialeah, FL (United States)

Additional Details

Clinical Investigator (CI)

Citations

IDCFRDescription
755221 CFR 312.66Changes in research
756021 CFR 312.60FD-1572, protocol compliance