FDA Inspection 701509 — Cleartooth Electronics, Inc.

Cleartooth Electronics, Inc. — FEI 3008313821

The FDA completed an inspection of Cleartooth Electronics, Inc. on Dec 9, 2010 in Boulder, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 9, 2010
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Boulder, CO (United States)