FDA Inspection 566801 - Covidien, LLC - February 23, 2009

FDA Inspection 566801 for Covidien, LLC on February 23, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 566801 for Covidien, LLC on February 23, 2009. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.50(a)(2)

21 CFR 820.100(a)(3)

21 CFR 820.160(a)

21 CFR 820.20

21 CFR 820.25(b)

21 CFR 820.30(c)

21 CFR 820.30(g)

21 CFR 820.75(a)

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Record Information

Company

Covidien, LLC

Inspection Date

February 23, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fd3a7cd5-f0e0-44cb-886b-98077f677e69

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