# FDA Inspection 942581 - PneumRx, Inc. - September 20, 2015

Source: https://www.keypedia.com/records/fda_inspections/pneumrx-inc/1dcf2eaf-4609-4e01-bbeb-f75ce09eedd8
Source feed: FDA_Inspections

> FDA Inspection 942581 for PneumRx, Inc. on September 20, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 942581
- Company Name: PneumRx, Inc.
- Inspection Date: 2015-09-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

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- [FDA Inspection 901292 - 2014-10-16](https://www.keypedia.com/records/fda_inspections/pneumrx-inc/194dc277-622b-40b8-8b58-6d3d85c76745)
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Company: https://www.keypedia.com/companies/pneumrx-inc/462c77c1-f107-4728-8edf-e72f2321cd5d

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