FDA Inspection 1026836 — Otoki Corporation Daepoong Factory

Otoki Corporation Daepoong Factory — FEI 3009934446

The FDA completed an inspection of Otoki Corporation Daepoong Factory on September 18, 2017 in Umseong-gun. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 6 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 18, 2017
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Umseong-gun (Korea (the Republic of))

Citations

IDCFRDescription
131621 CFR 113.87(c)Initial temperature of container contents
133021 CFR 113.100(a)Process records - forms missing information
164321 CFR 113.100(e)Incomplete information
288721 CFR 113.40(j)Processing: conform to other systems
387421 CFR 113.60(b)Cooling water - not chlorinated, sanitized
387721 CFR 113.60(c)Coding - required elements