FDA Inspection 1052089 — URCIMAR

URCIMAR — FEI 3004286359

The FDA completed an inspection of URCIMAR on May 16, 2018 in Fes. 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). 3 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 16, 2018
Fiscal Year
2018
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Fes (Morocco)

Citations

IDCFRDescription
128921 CFR 110.20(a)(3)Drainage
142221 CFR 110.20(b)(4)Floors, walls and ceilings
170221 CFR 110.80(b)(8)Metal / extraneous materials