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FDA Inspection 655126 — Ronald D. Berger, MD

Ronald D. Berger, MD — FEI 3008268995

The FDA completed an inspection of Ronald D. Berger, MD on Mar 23, 2010 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
Mar 23, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Baltimore, MD (United States)

Additional Details

Clinical Investigator (CI)

Facility

FDA data resources