FDA Inspection 1076413 — Daki, Ltee.

Daki, Ltee. — FEI 3008262698

The FDA completed an inspection of Daki, Ltee. on Jan 16, 2019 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). 6 citations were issued during this inspection. Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jan 16, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Boucherville (Canada)

Citations

IDCFRDescription
110521 CFR 211.22(d)Procedures not in writing, fully followed
111121 CFR 211.25(a)Training , Education , Experience overall
121321 CFR 211.67(a)Cleaning / Sanitizing / Maintenance
191421 CFR 211.166(a)Lack of written stability program
355921 CFR 211.56(a)Sanitation--buildings not clean, free of infestation
434221 CFR 211.142(b)Storage under appropriate conditions

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