FDA Inspection 1018198 — PT. Muria Bahari Indonesia

PT. Muria Bahari Indonesia — FEI 3011280608

The FDA completed an inspection of PT. Muria Bahari Indonesia on Jul 18, 2017 in Kudus. 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). 2 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 18, 2017
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Kudus (Indonesia)

Citations

IDCFRDescription
600521 CFR 123.6(c)(6)Verification procedures - adequacy
96121 CFR 123.6(c)(3)Critical limits

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