Home / Companies / Eurofins Pharmaceutical Product Testing Belgium NV

Eurofins Pharmaceutical Product Testing Belgium NV FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

Eurofins Pharmaceutical Product Testing Belgium NV has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "Eurofins Pharmaceutical Product Testing Belgium NV" is on file.

What these totals cover: FDA records filed under the name "Eurofins Pharmaceutical Product Testing Belgium NV" and its spelling variant "Eurofins Pharmaceutical Product Testing Belgium".

Latest inspection: Mar 21, 2025 · VAI

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	0	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	2	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

Eurofins Pharmaceutical Product Testing Belgium NV's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Year	Inspections	OAI	Warning letters	Recall records	Class I
2026	0	0	0	0	0
2025	1	0	0	0	0
2024	0	0	0	0	0
2023	0	0	0	0	0
2022	0	0	0	0	0
2021	0	0	0	0	0
2020	0	0	0	0	0
2019	1	0	0	0	0
2018	0	0	0	0	0
2017	0	0	0	0	0

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Reviewing Eurofins Pharmaceutical Product Testing Belgium NV as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Eurofins Pharmaceutical Product Testing Belgium NV yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

Recent FDA inspections

2 inspections from Aug 2, 2019 to Mar 21, 2025.

Date	Site	Product	Classification	FEI
Mar 21, 2025	Nazareth, Belgium	Drugs	Voluntary Action Indicated (VAI)	3012626551
Aug 2, 2019	Nazareth, Belgium	Drugs	Voluntary Action Indicated (VAI)	3012626551

NAI: No objectionable conditions or practices were found during the inspection.
VAI: Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI: Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3012626551	Nazareth, Belgium	2	Mar 21, 2025

Eurofins Pharmaceutical Product Testing Belgium NV and the FDA: common questions

Has Eurofins Pharmaceutical Product Testing Belgium NV received an FDA warning letter?

No FDA warning letter addressed to the name "Eurofins Pharmaceutical Product Testing Belgium NV" is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has Eurofins Pharmaceutical Product Testing Belgium NV received an FDA Form 483?

FDA has not published a Form 483 for "Eurofins Pharmaceutical Product Testing Belgium NV" in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect Eurofins Pharmaceutical Product Testing Belgium NV?

The most recent FDA inspection on file ended Mar 21, 2025 at Nazareth, Belgium and was classified VAI. FDA has 2 inspections of Eurofins Pharmaceutical Product Testing Belgium NV on file.

Need more than this page shows? Ask about Eurofins Pharmaceutical Product Testing Belgium NV in Claude or ChatGPT and get every site's inspections, Form 483s, warning letters and import alerts, with a link to the FDA source for each record. The API key is free: no card.