FDA Inspection 865848 — Humberto I. Aguilar

Humberto I. Aguilar — FEI 3010624029

The FDA completed an inspection of Humberto I. Aguilar on Feb 13, 2014 in Shreveport, LA. 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
Feb 13, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Shreveport, LA (United States)

Additional Details

Clinical Investigator (CI)