FDA Inspection 807195 — Omni-Guide Holdings, Inc.

Omni-Guide Holdings, Inc. — FEI 3005350457

The FDA completed an inspection of Omni-Guide Holdings, Inc. on November 15, 2012 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
November 15, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Billerica, MA (United States)