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

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Record Details

This FDA Inspection record concerns Calapro Inc Dba Calatex Inc, with an inspection on August 21, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Calapro Inc Dba Calatex Inc
Inspection Date: August 21, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · c73cd9f5-6956-4570-b7cf-1a32908acf14

Violation Codes3

21 CFR 803.1721 CFR 820.100(a)21 CFR 820.198(a)

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