FDA Inspection 1028532 — Carroll, John D.

Carroll, John D. — FEI 3013794389

The FDA completed an inspection of Carroll, John D. on September 14, 2017 in Aurora, CO. 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
September 14, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Aurora, CO (United States)

Additional Details

Clinical Investigator (CI)