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Bausch & Lomb Incorporated — FDA Facility Profile

FEI 1000119305

Bausch & Lomb Incorporated is an FDA-registered facility (FEI 1000119305) located in Manchester, MO, US. RegDataLab tracks 4 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Oct 10, 2019: No Action Indicated (NAI)
Inspections on record
4 (4 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
Import refusals
2

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
Oct 10, 2019No Action Indicated (NAI)No citations listed
Jun 9, 2016No Action Indicated (NAI)No citations listed
Apr 28, 2014No Action Indicated (NAI)No citations listed
Jan 19, 2012No Action Indicated (NAI)No citations listed

Facility details

Company
Bausch & Lomb, Inc.
Location
Manchester, MO (US)
Source
device

Import refusals

FDA data resources

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