FDA Inspection 1160466 — NEOLIGHT, LLC

NEOLIGHT, LLC — FEI 3014128880

The FDA completed an inspection of NEOLIGHT, LLC on Dec 17, 2021 in Scottsdale, AZ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 17, 2021
Fiscal Year
2022
Product Type
Devices
Project Area
Compliance: Devices
Location
Scottsdale, AZ (United States)