ZOETIS BELGIUM S.A — FDA Facility Profile

FEI 3015422006

ZOETIS BELGIUM S.A is an FDA-registered facility (FEI 3015422006) located in RATHDRUM, IE. Registered operations: ANALYSIS; API MANUFACTURE; MANUFACTURE; PARTICLE SIZE REDUCTION. RegDataLab tracks 2 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Jan 16, 2026: Voluntary Action Indicated (VAI)
Inspections on record
2 (2 VAI)
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

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
Jan 16, 2026Voluntary Action Indicated (VAI)No citations listed
Mar 25, 2022Voluntary Action Indicated (VAI)No citations listed

Facility details

Company
Zoetis Belgium S.A.
Location
RATHDRUM (IE)
Registration Expires
Dec 31, 2026
Operations
ANALYSIS; API MANUFACTURE; MANUFACTURE; PARTICLE SIZE REDUCTION
Source
decrs

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