FDA Inspection 830967 — Neptune Manufacturing Inc

Neptune Manufacturing Inc — FEI 3001554385

The FDA completed an inspection of Neptune Manufacturing Inc on May 15, 2013 in Los Angeles, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). 11 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
May 15, 2013
Fiscal Year
2013
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Los Angeles, CA (United States)

Citations

IDCFRDescription
152421 CFR 123.11(b)Sanitation monitoring
600421 CFR 123.6(c)(4)Monitoring - adequacy
600521 CFR 123.6(c)(6)Verification procedures - adequacy
600821 CFR 123.8(a)(3)Verification - record review - frequency
602021 CFR 123.9(a)Records - content
90521 CFR 123.6(b)HACCP plan implementation
93321 CFR 123.8(a)(2)(ii)Calibration - adequacy
95921 CFR 123.6(c)(1)Food safety hazards
96021 CFR 123.6(c)(2)Critical control points
96121 CFR 123.6(c)(3)Critical limits
96321 CFR 123.6(c)(5)Corrective action plan