FDA Inspection 1067116 — Richard I. Rothstein

Richard I. Rothstein — FEI 3014630002

The FDA completed an inspection of Richard I. Rothstein on Sep 7, 2018 in Lebanon, NH. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 7, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Lebanon, NH (United States)

Additional Details

Clinical Investigator (CI)