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Skretting Canada Inc. FDA Inspection Record

FEI 1000213448 · Inspections, Form 483s, warning letters and import refusals

Skretting Canada Inc. is an FDA-registered facility (FEI 1000213448) located in Vancouver, CA. Registered operations: MEDICATED ANIMAL FEED MANUFACTURE. RegDataLab tracks 4 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Sep 19, 2017: Voluntary Action Indicated (VAI)
Inspections on record
4 (3 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
Recalls as the recalling firm
1, latest May 8, 2007
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
Sep 19, 2017Voluntary Action Indicated (VAI)Vermin and pest infestation (21 CFR 225.120)
May 22, 2015No Action Indicated (NAI)No citations listed
Apr 24, 2012Voluntary Action Indicated (VAI)Maintain building to minimize pests (21 CFR 225.20(b)(3))
Assay results out of specification (21 CFR 225.58(d))
Distribution discontinued and control procedures established (21 CFR 225.58(e))
Jun 10, 2010Voluntary Action Indicated (VAI)Building grounds maintenance (21 CFR 225.20(b)(1))
Maintain building to minimize pests (21 CFR 225.20(b)(3))
Equipment maintenance & cleanliness (21 CFR 225.30(b)(2))
Three assays per year (21 CFR 225.58(b)(1))
and 3 more

Recalls

Newest first. Recalls FDA's Enforcement Report lists with this FEI as the recalling firm. The recalling firm is not always the site that made the product. Search FDA's Enforcement Report by recall number.

DateClassRecallProduct and reason
May 8, 2007Class IIIV-456-2007Fish feed - non-medicated and medicated; BioOregon label applied to all BioClarks… and 24 more products
Product contaminated with melamine

FDA record score

2 of 100. A count of this site's adverse public FDA records, weighted by how recent each one is. A higher number means more, or more recent, records. Each record below adds the points shown.

Counted on Nov 15, 2026, method version 1. It counts records and does not judge the site: a low number does not establish that a site is safe, and sites that FDA inspects more often can collect more points. How this is counted.

3 records behind this number
RecordDatePoints x age weightAdds
Inspection classified VAISep 19, 20176 x 0.251.5
Inspection classified VAIApr 24, 201210 years or older, so it adds no points0
Inspection classified VAIJun 10, 201010 years or older, so it adds no points0

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 15, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 14, 2026Newest record Nov 5, 2026Current
Compliance actions (warning letters, injunctions and other action types)Nov 2, 2026Newest record Oct 29, 2026Current
Warning letter textNov 14, 2026Newest record Nov 10, 2026Current
Recalls (Enforcement Report)Nov 14, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 2, 2026Newest record Oct 22, 2026Current

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Facility details

Company
Skretting Canada Inc
Location
Vancouver (CA)
Registration Expires
Dec 31, 2026
Operations
MEDICATED ANIMAL FEED MANUFACTURE
Source
decrs

Import refusals

FDA data resources

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