FDA Inspection 772729 — Perio Protect LLC

Perio Protect LLC — FEI 3005167547

The FDA completed an inspection of Perio Protect LLC on Mar 8, 2012 in Saint Louis, MO. 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). 7 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 8, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Saint Louis, MO (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
235021 CFR 820.25(b)Training - Lack of or inadequate procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
316821 CFR 820.198(a)Complaints
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures
50221 CFR 820.60Identification procedures, Lack of or inadequate procedures