FDA Inspection 955774 — Rhode Island Novelty Inc.

Rhode Island Novelty Inc. — FEI 3009761554

The FDA completed an inspection of Rhode Island Novelty Inc. on Jan 6, 2016 in Fall River, 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
Jan 6, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Fall River, MA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
63021 CFR 803.17Lack of Written MDR Procedures