FDA Inspection 857182 — Neptune Manufacturing Inc

Neptune Manufacturing Inc — FEI 3001554385

The FDA completed an inspection of Neptune Manufacturing Inc on Dec 20, 2013 in Los Angeles, CA. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). 11 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Dec 20, 2013
Fiscal Year
2014
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Los Angeles, CA (United States)

Citations

IDCFRDescription
142221 CFR 110.20(b)(4)Floors, walls and ceilings
152421 CFR 123.11(b)Sanitation monitoring
169521 CFR 110.80(b)(2)Manufacturing conditions
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
601821 CFR 123.7(a)Corrective action per predetermined plan
90521 CFR 123.6(b)HACCP plan implementation
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

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