FDA Inspection 972512 — Avacen Inc.

Avacen Inc. — FEI 3009668937

The FDA completed an inspection of Avacen Inc. on April 29, 2016 in Carlsbad, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 29, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Carlsbad, CA (United States)

Citations

IDCFRDescription
328521 CFR 820.90(b)(2)Product rework procedures, Lack of or inadequate procedures