FDA Inspection 1110471 — NEDERLAND USA INC

NEDERLAND USA INC — FEI 3014871787

The FDA completed an inspection of NEDERLAND USA INC on Nov 19, 2019 in Chicago, IL. 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
Nov 19, 2019
Fiscal Year
2020
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Chicago, IL (United States)

Additional details

FSVP

Citations

IDCFRDescription
1828321 CFR 1.505(b)Supplier approval - document
1829021 CFR 1.506(a)(1)Approved supplier procedures - importer established
1829321 CFR 1.506(b)Supplier verification - establish written procedures
1829621 CFR 1.506(d)(1)(i)Verification activity frequency

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