FDA Inspection 1248487 — WEERO CO LTD

WEERO CO LTD — FEI 3016087653

The FDA completed an inspection of WEERO CO LTD on Sep 5, 2024 in Suwon. 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). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 5, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Suwon (Korea (the Republic of))

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation
48621 CFR 820.50(a)Evaluation of suppliers, contractors, etc., requirements