FDA Inspection 945515 — Neptune Manufacturing Inc

Neptune Manufacturing Inc — FEI 3001554385

The FDA completed an inspection of Neptune Manufacturing Inc on Oct 29, 2015 in Los Angeles, CA. 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). 4 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 29, 2015
Fiscal Year
2016
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
600621 CFR 123.6(c)(7)Records values/observations
90521 CFR 123.6(b)HACCP plan implementation

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