Pulmodyne Inc.

Form 483

Indianapolis, Indiana, United StatesFEI 1832562Issued February 10, 2010

View FDA's Record for This Firm

Source: FDA inspection record. Confirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months. To check it, open FDA's record for this establishment on FDA's Data Dashboard, listed under FEI 1832562.

Observations1

Issue DateFebruary 10, 2010

StatusNo Warning Letter

Related Inspections5

Establishment Details

Firm: Pulmodyne Inc.
Location: Indianapolis, Indiana, United States
FEI Number: 1832562
Product Type: Devices
Issue Date: February 10, 2010
Country: United States

Inspection History, 2010 to 2025

NAI1

VAI3

OAI1

NAI means No Action Indicated. VAI means Voluntary Action Indicated. OAI means Official Action Indicated.

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Pulmodyne Inc. FDA Form 483, Indianapolis, Indiana, February 10, 2010