FDA Inspection 811158 — Acra Cut, Inc.

Acra Cut, Inc. — FEI 1220724

The FDA completed an inspection of Acra Cut, Inc. on December 14, 2012 in Acton, MA. 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
December 14, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Acton, MA (United States)

Citations

IDCFRDescription
317221 CFR 820.198(c)Investigation of device failures