FDA Inspection 1065229 — Gebelein Group Inc.

Gebelein Group Inc. — FEI 1210368

The FDA completed an inspection of Gebelein Group Inc. on September 11, 2018 in Hyde Park, MA. 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: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 11, 2018
Fiscal Year
2018
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Hyde Park, MA (United States)

Citations

IDCFRDescription
1903021 CFR 117.130(a)(1)Hazard Analysis - Identification of Hazard
1904521 CFR 117.160(a)Process controls - Validation
1905021 CFR 117.145(b)Allergen Controls - Monitoring Frequency