# Pulmodyne Inc. – FDA Inspection, Mar 22, 2013

Source: https://www.keypedia.com/records/fda_inspections/pulmodyne-inc/8dd0ab47-b1f6-4e0e-930e-06b7c41f9587
Source feed: FDA_Inspections

> FDA inspection 823725 of Pulmodyne Inc., March 22, 2013. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR parts 806 and 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 823725
- Company Name: Pulmodyne Inc.
- Inspection Date: 2013-03-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

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- FDA Inspection 1039908 - 2018-01-10
- [FDA Inspection 941634 - 2015-09-02](https://www.keypedia.com/records/fda_inspections/pulmodyne-inc/71ea0982-0ba9-47e6-94b9-61159481fbb0)
- [FDA Inspection 644965 - 2010-02-10](https://www.keypedia.com/records/fda_inspections/pulmodyne-inc/5966aa05-0da8-486c-b9c4-55024c5bc24e)

Company: https://www.keypedia.com/companies/pulmodyne-inc/8c17b704-2050-4c41-977d-f2141366a299

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7