FDA Inspection 733405 - OraWell USA - August 05, 2011

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Record Details

This FDA Inspection record concerns OraWell USA, with an inspection on August 5, 2011, issued by the Center for Devices and Radiological Health, covering devices.

Company: OraWell USA
Inspection Date: August 5, 2011
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · ad879b1c-1d07-4f9b-afbc-bd5454491e63

Violation Codes10

21 CFR 820.100(a)21 CFR 820.18121 CFR 820.18421 CFR 820.198(a)21 CFR 820.20(a)21 CFR 820.20(d)21 CFR 820.30(b)21 CFR 820.4021 CFR 820.50(b)21 CFR 820.70(a)

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