# PneumRx, Inc. – FDA Inspection, Sep 20, 2015

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

> FDA inspection 942581 of PneumRx, Inc., September 20, 2015. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 812. 3 other FDA inspections on record for this company.

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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)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Documents

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- [FDA Inspection 741996 - 2011-08-23](https://www.keypedia.com/records/fda_inspections/pneumrx-inc/6d18f30e-b781-4bef-8e4c-8fd7fdb0119d)

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