FDA Inspection 1107064 — Francisco Munoz, M.D.

Francisco Munoz, M.D. — FEI 3004785717

The FDA completed an inspection of Francisco Munoz, M.D. on October 10, 2019 in Elizabeth, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 10, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Elizabeth, NJ (United States)

Additional Details

Clinical Investigator (CI)