FDA Inspection 834006 — Cogmedix, Inc.

Cogmedix, Inc. — FEI 3007712511

The FDA completed an inspection of Cogmedix, Inc. on May 31, 2013 in West Boylston, MA. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 31, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
West Boylston, MA (United States)

Citations

IDCFRDescription
313021 CFR 820.100(a)Lack of or inadequate procedures