FDA Inspection 792116 — Laser Peripherals LLC

Laser Peripherals LLC — FEI 1221543

The FDA completed an inspection of Laser Peripherals LLC on Jul 27, 2012 in Plymouth, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 27, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Plymouth, MN (United States)

Citations

IDCFRDescription
73221 CFR 803.50(a)(2)Individual Report of Malfunction