FDA Inspection 1077106 — Avmor Ltd.

Avmor Ltd. — FEI 3003101044

The FDA completed an inspection of Avmor Ltd. on Jan 25, 2019 in Laval. 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 25, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Laval (Canada)

Citations

IDCFRDescription
360321 CFR 211.160(b)Scientifically sound laboratory controls

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