FDA Inspection 1087852 — Viking Rubber Products Inc.

Viking Rubber Products Inc. — FEI 3011660924

The FDA completed an inspection of Viking Rubber Products Inc. on April 29, 2019 in San Clemente, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 29, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
San Clemente, CA (United States)

Citations

IDCFRDescription
311821 CFR 820.75(a)Documentation
312521 CFR 820.80(d)Lack of or inadequate final acceptance procedures
315921 CFR 820.184DHR content