FDA Inspection 555077 — Solos Endoscopy Inc.

Solos Endoscopy Inc. — FEI 1000120488

The FDA completed an inspection of Solos Endoscopy Inc. on Nov 21, 2008 in Westport, 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
Nov 21, 2008
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Westport, CT (United States)