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Ribon Company, Ltd. FDA Inspection Record

FEI 3010493762 · Inspections, Form 483s, warning letters and import refusals

Ribon Company, Ltd. is an FDA-inspected facility (FEI 3010493762) located in Komaki, JP. RegDataLab tracks 2 FDA inspections and 1 compliance action at this facility.

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What FDA found at this site

Latest inspection
Feb 8, 2019: No Action Indicated (NAI)
Inspections on record
2 (1 OAI, 1 NAI)
Last OAI inspection
Feb 20, 2015
Warning letters
1 listed by FDA for this FEI, latest Oct 5, 2015
Import refusals
10 or more

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Feb 8, 2019No Action Indicated (NAI)No citations listed
Feb 20, 2015Official Action Indicated (OAI)No citations listed

Facility details

Company
Ribon Company, Ltd.
Location
Komaki (JP)
Source
inspections

Compliance actions

Import refusals

FDA data resources

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