FDA Inspection 771196 — Neptune Manufacturing Inc

Neptune Manufacturing Inc — FEI 3001554385

The FDA completed an inspection of Neptune Manufacturing Inc on Mar 2, 2012 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). 8 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 2, 2012
Fiscal Year
2012
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Los Angeles, CA (United States)

Citations

IDCFRDescription
152421 CFR 123.11(b)Sanitation monitoring
601021 CFR 123.8(a)(3)(i)Monitoring record review adequacy
602021 CFR 123.9(a)Records - content
90521 CFR 123.6(b)HACCP plan implementation
92921 CFR 123.8(b)Verification - corrective action
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.