FDA Inspection 1220916 — Laboratoire Du-Var Inc.

Laboratoire Du-Var Inc. — FEI 3002449500

The FDA completed an inspection of Laboratoire Du-Var Inc. on Oct 20, 2023 in Boucherville. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 4 citations were issued during this inspection. Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 20, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Boucherville (Canada)

Citations

IDCFRDescription
104921 CFR 211.22(a)Approve or reject components, products
136121 CFR 211.100(a)Absence of Written Procedures
202721 CFR 211.192Investigations of discrepancies, failures
430321 CFR 211.67(b)Written procedures fail to include

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