FDA Inspection 849776 — Kaasmakerij De Jong B.V.

Kaasmakerij De Jong B.V. — FEI 3003856868

The FDA completed an inspection of Kaasmakerij De Jong B.V. on Sep 2, 2013 in Alphen Nb. 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). Product area: Food/Cosmetics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 2, 2013
Fiscal Year
2013
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Alphen Nb (Netherlands)

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