FDA Inspection 586318 — Vertos Medical, Inc.

Vertos Medical, Inc. — FEI 3006450448

The FDA completed an inspection of Vertos Medical, Inc. on May 26, 2009 in Aliso Viejo, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 26, 2009
Fiscal Year
2009
Product Type
Devices
Project Area
Compliance: Devices
Location
Aliso Viejo, CA (United States)

Citations

IDCFRDescription
312521 CFR 820.80(d)Lack of or inadequate final acceptance procedures
369021 CFR 820.100(a)(3)Identification of actions needed