FDA Inspection 1020097 — Antonio E. Terrelonge

Antonio E. Terrelonge — FEI 3013525731

The FDA completed an inspection of Antonio E. Terrelonge on Jul 20, 2017 in Miami Springs, FL. 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
Jul 20, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Miami Springs, FL (United States)

Additional details

Clinical Investigator (CI)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.