FDA Inspection 1036682 — John J. Griffin, MD

John J. Griffin, MD — FEI 3003706321

The FDA completed an inspection of John J. Griffin, MD on December 20, 2017 in Virginia Beach, VA. 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
December 20, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Virginia Beach, VA (United States)

Additional Details

Clinical Investigator (CI)