# Transtracheal Systems, Inc. – FDA Inspection, Jul 31, 2009

Source: https://www.keypedia.com/records/fda_inspections/transtracheal-systems-inc/c5a2b9cf-ba64-4342-96da-41b500f745c3
Source feed: FDA_Inspections

> FDA inspection 600018 of Transtracheal Systems, Inc., July 31, 2009. Classification: Voluntary Action Indicated (VAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 600018
- Company Name: Transtracheal Systems, Inc.
- Inspection Date: 2009-07-31
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1129440 - 2020-09-17](https://www.keypedia.com/records/fda_inspections/transtracheal-systems-inc/e1a1e09b-93f6-46ca-9b0e-0a456319bb88)
- [FDA Inspection 1087542 - 2019-04-26](https://www.keypedia.com/records/fda_inspections/transtracheal-systems-inc/9ae89cc3-d125-4f33-9965-b04922637a89)
- FDA Inspection 819440 - 2013-02-19

Company: https://www.keypedia.com/companies/transtracheal-systems-inc/f8d29609-2d07-4dfc-a459-b1a926827613

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