FDA Inspection 1222097 — Taisho Pharmaceutical (M) SDN BHD

Taisho Pharmaceutical (M) SDN BHD — FEI 3004404787

The FDA completed an inspection of Taisho Pharmaceutical (M) SDN BHD on Nov 2, 2023 in Bandar Baru Bangi. 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). 5 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 2, 2023
Fiscal Year
2024
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Bandar Baru Bangi (Malaysia)

Citations

IDCFRDescription
1557921 CFR 111.155(c)(1)Components - representative samples
1582921 CFR 111.70(b)(1)Specifications - component identity
1585821 CFR 111.75(a)(1)(i)Component - verify identity, dietary ingredient
1586121 CFR 111.75(a)(2)(ii)(A)Component - qualify supplier
446421 CFR 108.25(c)(1)Registration

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