FDA Inspection 630365 — Infraredx, Inc.

Infraredx, Inc. — FEI 3015551113

The FDA completed an inspection of Infraredx, Inc. on October 29, 2009 in Bedford, 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
October 29, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Bedford, MA (United States)