FDA Inspection 979217 — Alfredo M. Carbonell

Alfredo M. Carbonell — FEI 3012527381

The FDA completed an inspection of Alfredo M. Carbonell on July 20, 2016 in Greenville, SC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 20, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Greenville, SC (United States)

Additional Details

Clinical Investigator (CI)