# FDA Inspection 871960 - Pneumex, Inc. - February 19, 2014

Source: https://www.keypedia.com/records/fda_inspections/pneumex-inc/47b89fc8-b40a-4b41-ab40-92a7525fd007
Source feed: FDA_Inspections

> FDA Inspection 871960 for Pneumex, Inc. on February 19, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 871960
- Company Name: Pneumex, Inc.
- Inspection Date: 2014-02-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 871960 - 2014-02-19](https://www.keypedia.com/records/fda_inspections/pneumex-inc/d74d5e14-0d4e-429a-a4c0-79dc29706eee)
- [FDA Inspection 736172 - 2011-07-07](https://www.keypedia.com/records/fda_inspections/pneumex-inc/fe71f21b-0ec2-4d83-a75a-e88ed65f0d63)

Company: https://www.keypedia.com/companies/pneumex-inc/b886a0c0-4acd-413d-b274-4d3fa2181a6e

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