FDA Inspection 1100420 - Calapro Inc Dba Calatex Inc - August 21, 2019

FDA Inspection 1100420 for Calapro Inc Dba Calatex Inc on August 21, 2019. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1100420 for Calapro Inc Dba Calatex Inc on August 21, 2019. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.100(a)

21 CFR 820.198(a)

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Record Information

Company

Calapro Inc Dba Calatex Inc

Inspection Date

August 21, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f7d5e1de-1157-40f8-91ab-33ae6e7b2bab

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