FDA Inspection 1069716 - Greiner Bio-One GmbH - October 25, 2018

FDA Inspection 1069716 for Greiner Bio-One GmbH on October 25, 2018. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 1069716 for Greiner Bio-One GmbH on October 25, 2018. Classification: Official Action Indicated (OAI).

Violation Codes

21 CFR 803.17

21 CFR 820.100(a)

21 CFR 820.198(a)

21 CFR 820.30(a)

21 CFR 820.50(a)(2)

21 CFR 820.75(a)

21 CFR 820.75(c)

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Record Information

Company

Greiner Bio-One GmbH

Inspection Date

October 25, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: c998d201-79b4-4c1e-916b-2e6be589cec0

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