FDA WARNING_LETTER - Steritec Products, Inc. - May 15, 2008

FDA WARNING_LETTER for Steritec Products, Inc. on May 15, 2008. Product: Devices. Access full analysis and detailed observations.

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Record Summary

FDA WARNING_LETTER for Steritec Products, Inc. on May 15, 2008. Product: Devices. Access full analysis and detailed observations.

Violation Codes

21 CFR 820.22

21 CFR 820.30(i)

21 CFR 820.100

21 U.S.C. 321(h)

21 CFR 820.80(b)

21 CFR 820.30(d)

21 CFR 820.5

21 CFR 820.75(a)

21 U.S.C. 351(h)

21 CFR 820.30(g)

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Record Information

Company

Steritec Products, Inc.

Inspection Date

May 15, 2008

Product Type

Devices

Office

Denver District Office

People

Thomas Warwick (H.)

ID: 81af4e76-f219-4c84-b4da-b48573b35f13

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