Bunge North America, Inc - Soybean Process Division FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Bunge North America, Inc - Soybean Process Division has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Bunge North America, Inc - Soybean Process Division" is on file.

What these totals cover: FDA records filed under the name "Bunge North America, Inc - Soybean Process Division".

Latest inspection
Aug 1, 2011 · NAI

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections1Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

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Recent FDA inspections

1 inspection on Aug 1, 2011.

DateSiteProductClassificationFEI
Aug 1, 2011Marks, MSVeterinaryNo Action Indicated (NAI)1030864
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 1030864Marks, MS1Aug 1, 2011

Bunge North America, Inc - Soybean Process Division and the FDA: common questions

Has Bunge North America, Inc - Soybean Process Division received an FDA warning letter?

No FDA warning letter addressed to the name "Bunge North America, Inc - Soybean Process Division" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Bunge North America, Inc - Soybean Process Division received an FDA Form 483?

FDA has not published a Form 483 for "Bunge North America, Inc - Soybean Process Division" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Bunge North America, Inc - Soybean Process Division?

The most recent FDA inspection on file ended Aug 1, 2011 at Marks, MS and was classified NAI. FDA has 1 inspection of Bunge North America, Inc - Soybean Process Division on file.

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