FDA Inspection 1050577 — Neptune Manufacturing Inc

Neptune Manufacturing Inc — FEI 3001554385

The FDA completed an inspection of Neptune Manufacturing Inc on May 3, 2018 in Los Angeles, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 6 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
May 3, 2018
Fiscal Year
2018
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Los Angeles, CA (United States)

Citations

IDCFRDescription
10005n/aProcedural requirements
142221 CFR 110.20(b)(4)Floors, walls and ceilings
600721 CFR 123.9(a)Records entries - timing
601821 CFR 123.7(a)Corrective action per predetermined plan
90521 CFR 123.6(b)HACCP plan implementation
93321 CFR 123.8(a)(2)(ii)Calibration - adequacy