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FDA Inspection 997999 — Omni-Guide Holdings, Inc.

Omni-Guide Holdings, Inc. — FEI 3005350457

The FDA completed an inspection of Omni-Guide Holdings, Inc. on January 5, 2017 in Billerica, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 5, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Billerica, MA (United States)

Facility

Other inspections at this facility

  • 1177895 (VAI Fri Aug 19 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1009910 (VAI Tue May 02 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 888872 (NAI Thu Jul 24 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 807195 (NAI Thu Nov 15 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 765565 (NAI Mon Feb 13 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources