Home / Inspections / 682551

FDA Inspection 682551 — Neurotron. Inc.

Neurotron. Inc. — FEI 1121806

The FDA completed an inspection of Neurotron. Inc. on September 27, 2010 in Aurora, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 27, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Aurora, CO (United States)

Facility

Other inspections at this facility

  • 1007463 (VAI Mon Apr 10 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1007462 (VAI Mon Apr 10 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 799351 (NAI Tue Sep 18 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 798374 (NAI Wed Sep 12 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 554398 (NAI Wed Dec 17 2008 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources