FDA Inspection 1023339 — Lumen Photon Therapy Inc.

Lumen Photon Therapy Inc. — FEI 3004521629

The FDA completed an inspection of Lumen Photon Therapy Inc. on July 13, 2017 in Columbus, NC. 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
July 13, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Columbus, NC (United States)