FDA Inspection 1286530 — EIFFAGE Energie Systemes Electronique

EIFFAGE Energie Systemes Electronique — FEI 3035611132

The FDA completed an inspection of EIFFAGE Energie Systemes Electronique on Sep 16, 2025 in Verquin. 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). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 16, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Verquin (France)

Citations

IDCFRDescription
1471321 CFR 820.198(a)Lack of or inadequate complaint procedures
313021 CFR 820.100(a)Lack of or inadequate procedures
343321 CFR 820.75(c)Process changes - review, evaluation and revalidation

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