FDA Inspection 885093 — Skrepnik Nebosja MD

Skrepnik Nebosja MD — FEI 3010885594

The FDA completed an inspection of Skrepnik Nebosja MD on Jun 11, 2014 in Tucson, AZ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 11, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Tucson, AZ (United States)

Additional Details

Clinical Investigator (CI)