# FDA Inspection 721539 - Pulmonary Filtration Technologies - April 07, 2011

Source: https://www.globalkeysolutions.net/records/fda_inspections/pulmonary-filtration-technologies/ddf92edb-ceb3-41e4-a2fa-7aae043810c2
Source feed: FDA_Inspections

> FDA Inspection 721539 for Pulmonary Filtration Technologies on April 07, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 721539
- Company Name: Pulmonary Filtration Technologies
- Inspection Date: 2011-04-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 959076 - 2016-02-24](https://www.globalkeysolutions.net/records/fda_inspections/pulmonary-filtration-technologies/3670147b-b5f4-42b2-a3b1-dc7c2af83c2c)
- [FDA Inspection 721539 - 2011-04-07](https://www.globalkeysolutions.net/records/fda_inspections/pulmonary-filtration-technologies/1b2258b1-2712-4a8a-9385-07eb7a04b98b)

Company: https://www.globalkeysolutions.net/companies/pulmonary-filtration-technologies/e3fbd19c-e20d-40f7-880a-02e257c5bcc4

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