FDA Inspection 1116901 — SM Worldwide USA, Inc.

SM Worldwide USA, Inc. — FEI 3012970034

The FDA completed an inspection of SM Worldwide USA, Inc. on Feb 5, 2020 in Jamaica, NY. 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). 3 citations were issued during this inspection. Product area: Devices.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 5, 2020
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Jamaica, NY (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
63021 CFR 803.17Lack of Written MDR Procedures

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.