Ivy Animal Health Inc FDA Inspection Record

FEI 1910028 · Inspections, Form 483s, warning letters and import refusals

Ivy Animal Health Inc is an FDA-inspected facility (FEI 1910028) located in Overland Park, KS, US. RegDataLab tracks 7 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Apr 14, 2023: No Action Indicated (NAI)
Inspections on record
7 (3 VAI, 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
Recalls as the recalling firm
1, latest Nov 17, 2010

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
Apr 14, 2023No Action Indicated (NAI)No citations listed
Jun 17, 2019No Action Indicated (NAI)No citations listed
Aug 12, 2016No Action Indicated (NAI)No citations listed
Sep 23, 2013No Action Indicated (NAI)No citations listed
Apr 13, 2011Voluntary Action Indicated (VAI)Scientifically sound laboratory controls (21 CFR 211.160(b))
Establishment of calibration procedures (21 CFR 211.160(b)(4))
Oct 18, 2010Voluntary Action Indicated (VAI)Written procedures not established/followed (21 CFR 211.67(b))
SOPs not followed / documented (21 CFR 211.100(b))
Changes to Procedures Not Reviewed, Approved (21 CFR 211.100(a))
Feb 17, 2010Voluntary Action Indicated (VAI)Weights and Measures of Components Used (21 CFR 211.188(b)(4))
Investigations of discrepancies, failures (21 CFR 211.192)
Sanitation--buildings not clean, free of infestation (21 CFR 211.56(a))
Buildings not maintained in good state of repair (21 CFR 211.58)
and 7 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
Nov 17, 2010Class IIIV-100-2011VetLife Encore Estradiol, each silicone rubber implant contains 43.9 mg estradiol and is…
Recalling firm is initiating a voluntary recall as a precautionary measure due to the use of an ingredient from an approved supplier.

FDA record score

0 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 VAIApr 13, 201110 years or older, so it adds no points0
Inspection classified VAIOct 18, 201010 years or older, so it adds no points0
Inspection classified VAIFeb 17, 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 14, 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
Ivy Animal Health Inc
Location
Overland Park, KS (US)
Source
inspections

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