FDA Inspection 727422 — ITI LLC

ITI LLC — FEI 3007643940

The FDA completed an inspection of ITI LLC on May 10, 2011 in Middletown, 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
May 10, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Middletown, CT (United States)