FDA Inspection 1225054 — WHIRLPOOL EMEA SPA

WHIRLPOOL EMEA SPA — FEI 3014688442

The FDA completed an inspection of WHIRLPOOL EMEA SPA on Dec 15, 2023 in Biandronno. 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
Dec 15, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Biandronno (Italy)

Citations

IDCFRDescription
512321 CFR 1030.10(c)(3)(iv)Door position
594021 CFR 1030.10(c)(3)(i)tests--errors and uncertainties accounted for

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