Vetoquinol N.-A. INC FDA Inspection Record

FEI 3003510513 · Inspections, Form 483s, warning letters and import refusals

Vetoquinol N.-A. INC is an FDA-registered facility (FEI 3003510513) located in Princeville, CA. Registered operations: ANALYSIS; API MANUFACTURE; LABEL; MANUFACTURE; PACK. RegDataLab tracks 5 FDA inspections and 1 compliance action at this facility.

What FDA found at this site

Latest inspection
Aug 25, 2023: Voluntary Action Indicated (VAI)
Inspections on record
5 (5 VAI)
Last OAI inspection
None on record
Warning letters
1 listed by FDA for this FEI, latest Jun 29, 2017
Recalls as the recalling firm
1, latest Aug 17, 2010
Import refusals
5

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
Aug 25, 2023Voluntary Action Indicated (VAI)No citations listed
Jul 20, 2018Voluntary Action Indicated (VAI)Absence of Written Procedures (21 CFR 211.100(a))
Establish reliability of supplier's C of A (21 CFR 211.84(d)(2))
Status of Each Lot Identified (21 CFR 211.80(d))
Mar 31, 2017Voluntary Action Indicated (VAI)No citations listed
Mar 16, 2012Voluntary Action Indicated (VAI)Cleaning / Sanitizing / Maintenance (21 CFR 211.67(a))
Manufacturing Instructions and Specifications (21 CFR 211.186(b)(9))
Control procedures to monitor and validate performance (21 CFR 211.110(a))
Description of containers, labels, et. al. (21 CFR 211.186(b)(8))
May 18, 2010Voluntary Action Indicated (VAI)No citations listed

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
Aug 17, 2010Class IIIV-219-2010Oxytetracycline Hydrochloride Soluble Powder, For use in drinking water only, packaged in…
Foreign manufacturer of API was not approved.

FDA record score

14 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 14, 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.

6 records behind this number
RecordDatePoints x age weightAdds
Warning letter on FDA's dashboard, which does not show close-outsJun 29, 201730 x 0.257.5
Inspection classified VAIAug 25, 20236 x 0.63.6
Inspection classified VAIJul 20, 20186 x 0.251.5
Inspection classified VAIMar 31, 20176 x 0.251.5
Inspection classified VAIMar 16, 201210 years or older, so it adds no points0
Inspection classified VAIMay 18, 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
Vetoquinol N.-A. Inc.
Location
Princeville (CA)
Registration Expires
Dec 31, 2026
Operations
ANALYSIS; API MANUFACTURE; LABEL; MANUFACTURE; PACK
Source
decrs

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