FDA Inspection 814201 — Steven L. Zweibel

Steven L. Zweibel — FEI 3009773401

The FDA completed an inspection of Steven L. Zweibel on Jan 15, 2013 in Hartford, CT. 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
Jan 15, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Hartford, CT (United States)

Additional Details

Clinical Investigator (CI)