FDA Inspection 736527 — Arkray Factory USA, Inc.

Arkray Factory USA, Inc. — FEI 1832816

The FDA completed an inspection of Arkray Factory USA, Inc. on Jul 22, 2011 in Doral, 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 22, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Doral, FL (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures