FDA Inspection 995653 — Cerapedics, Inc.

Cerapedics, Inc. — FEI 3007155473

The FDA completed an inspection of Cerapedics, Inc. on December 9, 2016 in Westminster, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 9, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Westminster, CO (United States)

Additional Details

Postmarket Audit Inspections

Citations

IDCFRDescription
328521 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures
342521 CFR 820.50(a)(1)Evaluation and Selection, Suppliers, Contractors, etc.
54621 CFR 820.75(a)Lack of or inadequate process validation