FDA Inspection 1030246 — Dr. Johathan Grossberg

Dr. Johathan Grossberg — FEI 3013901425

The FDA completed an inspection of Dr. Johathan Grossberg on September 26, 2017 in Atlanta, GA. 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 26, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Atlanta, GA (United States)

Additional Details

Clinical Investigator (CI)