FDA Inspection 741461 — Isopure Corp.

Isopure Corp. — FEI 3013942511

The FDA completed an inspection of Isopure Corp. on Aug 25, 2011 in Louisville, KY. 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
Aug 25, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Louisville, KY (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation
419121 CFR 806.10(a)(1)Report of risk to health

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