Labverity
Facility profile

Pharmachemie B.V.

Testing & analysis · Drug product manufacturing · Haarlem · Netherlands

FDA recordFDA directory updated Jul 21, 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.

AnalysisLabelManufacturePackSterilize
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 21, 2026

Latest matched inspection
Voluntary action indicated (VAI)

Oct 17, 2024 · 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 history6 inspection records

FDA inspection history

6 records, Feb 2010 – Oct 2024 · 3 NAI · 3 VAI · 0 OAI

DateClassProject areaCitationsFY
Oct 17, 2024VAIDrug Quality Assurance2025
Sep 9, 2021NAIDrug Quality Assurance2021
May 17, 2019NAIDrug Quality Assurance2019
May 29, 2015NAIDrug Quality Assurance2015
Jun 28, 2013VAIDrug Quality AssuranceYes2013
Feb 19, 2010VAIDrug Quality Assurance2010

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