# FDA Inspection 839854 - Spiracle Technology - June 18, 2013

Source: https://www.keypedia.com/records/fda_inspections/spiracle-technology/09ee7dbc-6af5-41b6-95e8-7bb8716cd07a
Source feed: FDA_Inspections

> FDA Inspection 839854 for Spiracle Technology on June 18, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 839854
- Company Name: Spiracle Technology
- Inspection Date: 2013-06-18
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 839854 - 2013-06-18](https://www.keypedia.com/records/fda_inspections/spiracle-technology/b8beaae8-1466-4512-8647-f6dfba1c30bf)
- [FDA Inspection 577632 - 2009-04-17](https://www.keypedia.com/records/fda_inspections/spiracle-technology/e78d8ec5-59eb-4286-b174-21cfa3ad5eff)
- [FDA Inspection 577632 - 2009-04-17](https://www.keypedia.com/records/fda_inspections/spiracle-technology/6170297a-99a4-4d53-b07b-1eb4dbd09145)

Company: https://www.keypedia.com/companies/spiracle-technology/dc3fcdca-cdbe-4075-ae31-2bfac5f30a4c

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