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Facility profile

Les Importations Herbasante Inc

Drug product manufacturing · Active pharmaceutical ingredient (API) manufacturing · QC H4N 2L3 · Canada

FDA recordFDA directory updated Jul 21, 2026Profile not yet claimed
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Listed operations

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

Active pharmaceutical ingredient (API) manufactureManufacture
Due diligence

Regulatory record at a glance

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Registration record
Current FDA registration record

Expires Dec 31, 2026 · checked Jul 21, 2026

Latest matched inspection
Voluntary action indicated (VAI)

Dec 1, 2017 · FDA documented observations for voluntary correction.

Matched compliance actions
Warning Letter · Jan 2024

Within five years · review the action and follow-up.

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Shows

Registration status and a latest matched voluntary action indicated inspection.

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

FDA inspection history

3 records, Aug 2013 – Dec 2017 · 0 NAI · 3 VAI · 0 OAI

DateClassProject areaCitationsFY
Dec 1, 2017VAIDrug Quality AssuranceYes2018
Nov 5, 2015VAIDrug Quality Assurance2016
Aug 23, 2013VAIDrug Quality AssuranceYes2013

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

Matched compliance actions

Jan 31, 2024Warning Letter · CDER
Unclaimed profile

Service details not yet provided

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

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