FDA Inspection 823506 — UniDentalDirect, LLC

UniDentalDirect, LLC — FEI 3009162123

The FDA completed an inspection of UniDentalDirect, LLC on Mar 14, 2013 in Aventura, FL. 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). 9 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 14, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Aventura, FL (United States)

Citations

IDCFRDescription
1471221 CFR 820.184DHR - not or inadequately maintained
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
237121 CFR 820.30(a)Design control - no procedures
310121 CFR 820.30(g)Design validation- Lack of or inadequate procedures
312021 CFR 820.80(a)Lack of or inadequate procedures - Acceptance activities
313021 CFR 820.100(a)Lack of or inadequate procedures
313921 CFR 820.140Lack of or inadequate procedures for handling
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures