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Church & Dwight Canada Corp FDA Inspection Record

FEI 1000657351 · Inspections, Form 483s, warning letters and import refusals

Church & Dwight Canada Corp is an FDA-registered facility (FEI 1000657351) located in MONTREAL, QUEBEC, CA. Registered operations: MANUFACTURE; PACK. RegDataLab tracks 5 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Feb 7, 2025: Voluntary Action Indicated (VAI)
Inspections on record
5 (4 VAI, 1 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
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 7, 2025Voluntary Action Indicated (VAI)Procedures not in writing, fully followed (21 CFR 211.22(d))
Investigations of discrepancies, failures (21 CFR 211.192)
Jul 18, 2024No Action Indicated (NAI)No citations listed
Jan 17, 2020Voluntary Action Indicated (VAI)Procedures not in writing, fully followed (21 CFR 211.22(d))
Written records kept in individual logs (21 CFR 211.182)
Complete test data included in records (21 CFR 211.194(a))
Test method modification records not maintained (21 CFR 211.194(b))
and 2 more
Dec 8, 2017Voluntary Action Indicated (VAI)Procedures not in writing, fully followed (21 CFR 211.22(d))
Buildings not maintained in good state of repair (21 CFR 211.58)
Calibration - at intervals, written program, remedial action (21 CFR 211.160(b)(4))
Feb 26, 2016Voluntary Action Indicated (VAI)No citations listed

Facility details

Company
Church & Dwight Canada Corp.
Location
MONTREAL, QUEBEC (CA)
Registration Expires
Dec 31, 2026
Operations
MANUFACTURE; PACK
Source
both

Import refusals

FDA data resources

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