FDA Inspection 546390 - Brymill Corporation - November 07, 2008

FDA Inspection 546390 for Brymill Corporation on November 07, 2008. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 546390 for Brymill Corporation on November 07, 2008. Classification: Official Action Indicated (OAI).

Violation Codes

21 CFR 820.184

21 CFR 820.184(b)

21 CFR 820.198(c)

21 CFR 820.25(b)

21 CFR 820.30(f)

21 CFR 820.30(g)

21 CFR 820.50(a)(1)

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Record Information

Company

Brymill Corporation

Inspection Date

November 7, 2008

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fc991b81-a965-4274-b775-24f04a3d6887

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