BOURBON CORPORATION FDA Record

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

BOURBON CORPORATION has 0 FDA recalls, 9 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "BOURBON CORPORATION" is on file.

What these totals cover: FDA records filed under the name "BOURBON CORPORATION".

Latest inspection
Nov 1, 2018 · 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
Inspections9Nov 14, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

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Recent FDA inspections

9 inspections from Jul 8, 2014 to Nov 1, 2018.

DateSiteProductClassificationFEI
Nov 1, 2018Niigata, JapanFood/CosmeticsNo Action Indicated (NAI)3001251659
Jul 25, 2014Murakami, JapanFood/CosmeticsNo Action Indicated (NAI)3010119881
Jul 24, 2014Shibata, JapanFood/CosmeticsVoluntary Action Indicated (VAI)2000006693
Jul 22, 2014Gosen, JapanFood/CosmeticsNo Action Indicated (NAI)3004720236
Jul 18, 2014Niigata, JapanFood/CosmeticsVoluntary Action Indicated (VAI)3001251659
Jul 16, 2014Niigata, JapanFood/CosmeticsNo Action Indicated (NAI)2000006691
Jul 14, 2014Nagaoka, JapanFood/CosmeticsVoluntary Action Indicated (VAI)3006434625
Jul 10, 2014Joetsu, JapanFood/CosmeticsNo Action Indicated (NAI)2000006689
Jul 8, 2014Joetsu, JapanFood/CosmeticsVoluntary Action Indicated (VAI)2000006689
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

7 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3001251659Niigata, Japan2Nov 1, 2018
FEI 3010119881Murakami, Japan1Jul 25, 2014
FEI 2000006693Shibata, Japan1Jul 24, 2014
FEI 3004720236Gosen, Japan1Jul 22, 2014
FEI 2000006691Niigata, Japan1Jul 16, 2014
FEI 3006434625Nagaoka, Japan1Jul 14, 2014
FEI 2000006689Joetsu, Japan2Jul 10, 2014

BOURBON CORPORATION and the FDA: common questions

Has BOURBON CORPORATION received an FDA warning letter?

No FDA warning letter addressed to the name "BOURBON CORPORATION" 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 BOURBON CORPORATION received an FDA Form 483?

FDA has not published a Form 483 for "BOURBON CORPORATION" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect BOURBON CORPORATION?

The most recent FDA inspection on file ended Nov 1, 2018 at Niigata, Japan and was classified NAI. FDA has 9 inspections of BOURBON CORPORATION on file.

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