FDA Inspection 983251 — BioCeramics Restorative Materials

BioCeramics Restorative Materials — FEI 3009404424

The FDA completed an inspection of BioCeramics Restorative Materials on Aug 26, 2016 in Fort Lauderdale, 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). 4 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 26, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Fort Lauderdale, FL (United States)

Citations

IDCFRDescription
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
341521 CFR 820.22Quality Audit/Reaudit - conducted
366621 CFR 820.20(c)Management review - Lack of or inadequate procedures