FDA Inspection 1089368 - Flex-Cell Precision, Inc - March 27, 2019

FDA Inspection 1089368 for Flex-Cell Precision, Inc on March 27, 2019. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1089368 for Flex-Cell Precision, Inc on March 27, 2019. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.40

21 CFR 820.50(a)

21 CFR 820.75(a)

21 CFR 820.80(d)

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Record Information

Company

Flex-Cell Precision, Inc

Inspection Date

March 27, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ff270666-13f9-4a4b-9f3e-6f877fc8d7c5

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