FDA Inspection 1004056 — RJC Products

RJC Products — FEI 3007319157

The FDA completed an inspection of RJC Products on Feb 10, 2017 in Burnsville, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 10, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Burnsville, MN (United States)

Citations

IDCFRDescription
232821 CFR 820.22Quality audits - auditor independence
323521 CFR 820.72(a)Equipment control activity documentation
323621 CFR 820.72(b)Calibration procedures - content