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

Source: https://www.keypedia.com/records/fda_inspections/pulmodyne-inc/6cf0c771-83f1-41b6-a4ff-bd8dfd75635c
Source feed: FDA_Inspections

> FDA Inspection 823725 for Pulmodyne Inc. on March 22, 2013. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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