FDA Inspection 916075 — Vascular Pathways, Inc

Vascular Pathways, Inc — FEI 3009724479

The FDA completed an inspection of Vascular Pathways, Inc on Feb 25, 2015 in Boca Raton, 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). 6 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 25, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Boca Raton, FL (United States)

Citations

IDCFRDescription
1471821 CFR 820.30(g)Design validation - Risk analysis
232721 CFR 820.22Quality audits - Lack of or inadequate procedures
310321 CFR 820.30(i)Design changes - Lack of or Inadequate Procedures
311821 CFR 820.75(a)Documentation
313021 CFR 820.100(a)Lack of or inadequate procedures
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures