FDA Inspection 1111499 — WIDE USA CORPORATION

WIDE USA CORPORATION — FEI 3013397499

The FDA completed an inspection of WIDE USA CORPORATION on November 27, 2019 in Anaheim, 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
November 27, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Anaheim, CA (United States)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
44721 CFR 820.40Lack of procedures, or not maintained