FDA Inspection 900096 — AB RAHMS KEXFABRIK

AB RAHMS KEXFABRIK — FEI 3009768123

The FDA completed an inspection of AB RAHMS KEXFABRIK on Oct 17, 2014 in Hagersten. 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). 10 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 17, 2014
Fiscal Year
2015
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Hagersten (Sweden)

Citations

IDCFRDescription
129221 CFR 110.20(b)(1)Sufficient space
130621 CFR 110.20(b)(7)Screening
140221 CFR 110.10(b)(4)Unsecured jewelry
140521 CFR 110.10(b)(6)Failure to wear
142221 CFR 110.20(b)(4)Floors, walls and ceilings
156221 CFR 110.35(d)Failure to clean - general
169621 CFR 110.80(b)(3)Holding foods - refrigerate/freeze/heat
170821 CFR 110.80(b)(12)Batters, breading, gravies, sauces, etc.
239421 CFR 110.80(b)(6)Contamination by raw materials, refuse, other ingredients
98521 CFR 110.10(b)(1)Suitable outer garments

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