FDA Inspection 878416 — Ranfac Corporation

Ranfac Corporation — FEI 1211566

The FDA completed an inspection of Ranfac Corporation on May 6, 2014 in Avon, MA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 6, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Avon, MA (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation
73221 CFR 803.50(a)(2)Individual Report of Malfunction