FDA Inspection 867427 — Bartley Griffith, MD

Bartley Griffith, MD — FEI 3010647390

The FDA completed an inspection of Bartley Griffith, MD on Feb 24, 2014 in Baltimore, MD. 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
Feb 24, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Baltimore, MD (United States)

Additional Details

Clinical Investigator (CI)