FDA Inspection 1074774 — BIDOR KWONG HENG SDN BHD

BIDOR KWONG HENG SDN BHD — FEI 3013292592

The FDA completed an inspection of BIDOR KWONG HENG SDN BHD on Dec 12, 2018 in Bidor. 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). 6 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 12, 2018
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Bidor (Malaysia)

Citations

IDCFRDescription
1814121 CFR 117.35(a)Sanitary operations - Plant maintenance
1814521 CFR 117.35(c)Pest control
307121 CFR 114.80(a)(1)Scheduled process
307521 CFR 114.80(a)(4)Container testing
307821 CFR 114.80(b)Code - required elements
308821 CFR 114.100(b)Processing and production - required information

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.