Labverity
Facility profile

San'Up

Testing & analysis · Drug product manufacturing · Liege 4920 · Belgium

FDA recordFDA directory updated Jul 22, 2026Profile not yet claimed
Potential fit

Listed operations

The U.S. Food and Drug Administration (FDA) record lists broad activities for this site. Confirm specific services and availability directly.

AnalysisLabelManufacturePack
Due diligence

Regulatory record at a glance

Use these records to guide qualification; they are not a facility score.

Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 22, 2026

Latest matched inspection
Voluntary action indicated (VAI)

May 22, 2025 · FDA documented observations for voluntary correction.

Matched compliance actions
None in our records

No warning letter, injunction, or seizure matched.

Understand this record

Use the evidence, then ask for fit.

Shows

Registration status and a latest matched voluntary action indicated inspection.

Doesn’t show

Exact services, availability, capacity, pricing, or overall quality.

Ask next

Ask what was corrected and review any later inspection or follow-up record.

Method and source details
View full inspection and compliance history3 inspection records

FDA inspection history

3 records, Jan 2017 – May 2025 · 0 NAI · 3 VAI · 0 OAI

DateClassProject areaCitationsFY
May 22, 2025VAIDrug Quality Assurance2025
Dec 17, 2019VAIDrug Quality Assurance2020
Jan 27, 2017VAIDrug Quality AssuranceYes2017

No action indicated (NAI) · Voluntary action indicated (VAI) · Official action indicated (OAI)

Matched compliance actions

No warning letter, injunction, or seizure is matched in the current data set.

Unclaimed profile

Service details not yet provided

Methods, equipment, quality scope, capacity, turnaround, and commercial contacts are not available.

Ask about services