FDA Inspection 1101050 - Lantz Medical, Inc. - August 23, 2019

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Record Details

This FDA Inspection record concerns Lantz Medical, Inc., with an inspection on August 23, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Lantz Medical, Inc.
Inspection Date: August 23, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 78112d47-1712-4b10-b7a7-7f3ee0f1634b

Violation Codes7

21 CFR 820.100(a)21 CFR 820.18421 CFR 820.198(a)21 CFR 820.2221 CFR 820.30(g)21 CFR 820.30(j)21 CFR 820.90(a)

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