FDA Inspection 1054770 — Reavillmed, Llc

Reavillmed, Llc — FEI 3007306123

The FDA completed an inspection of Reavillmed, Llc on Apr 27, 2018 in Grayslake, IL. 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
Apr 27, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Grayslake, IL (United States)