FDA Inspection 1116000 — Laboratoires Delon

Laboratoires Delon — FEI 3002698327

The FDA completed an inspection of Laboratoires Delon on Jan 24, 2020 in Pointe-Claire. 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). 1 citation was issued during this inspection. Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 24, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Pointe-Claire (Canada)

Citations

IDCFRDescription
434221 CFR 211.142(b)Storage under appropriate conditions

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