FDA Inspection 637100 — Intelifuse Inc

Intelifuse Inc — FEI 3005509435

The FDA completed an inspection of Intelifuse Inc on Dec 23, 2009 in Metairie, LA. 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 23, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Metairie, LA (United States)

Citations

IDCFRDescription
341521 CFR 820.22Quality Audit/Reaudit - conducted