FDA Inspection 823725 - Pulmodyne Inc. - March 22, 2013

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Record Details

This FDA Inspection record concerns Pulmodyne Inc., with an inspection on March 22, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Pulmodyne Inc.
Inspection Date: March 22, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 6cf0c771-83f1-41b6-a4ff-bd8dfd75635c

Violation Codes4

21 CFR 806.10(a)(2)21 CFR 820.70(c)21 CFR 820.75(a)21 CFR 820.90(a)

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