FDA Inspection 926479 — Rms Surgical, Inc.

Rms Surgical, Inc. — FEI 3003661352

The FDA completed an inspection of Rms Surgical, Inc. on May 15, 2015 in Memphis, TN. 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). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 15, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Memphis, TN (United States)

Citations

IDCFRDescription
311821 CFR 820.75(a)Documentation
313021 CFR 820.100(a)Lack of or inadequate procedures
317221 CFR 820.198(c)Investigation of device failures
369621 CFR 820.100(b)Documentation