# FDA Inspection 608313 - Spentech, Inc. - August 26, 2009

Source: https://www.keypedia.com/records/fda_inspections/spentech-inc/b9d897b1-4b31-49d0-8ba8-ad8e1f2a460e
Source feed: FDA_Inspections

> FDA Inspection 608313 for Spentech, Inc. on August 26, 2009. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 608313
- Company Name: Spentech, Inc.
- Inspection Date: 2009-08-26
- 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 1020883 - 2017-07-27](https://www.keypedia.com/records/fda_inspections/spentech-inc/a0637e1a-dd7d-415f-b970-2a0a0962004f)
- [FDA Inspection 1020883 - 2017-07-27](https://www.keypedia.com/records/fda_inspections/spentech-inc/d0bb5cbc-1b58-451b-bc41-e2e435c58ef5)
- [FDA Inspection 912557 - 2015-02-04](https://www.keypedia.com/records/fda_inspections/spentech-inc/0c72dbeb-1ddb-4dfd-b452-2d105a60dce1)
- [FDA Inspection 912557 - 2015-02-04](https://www.keypedia.com/records/fda_inspections/spentech-inc/b4a8ef94-3b40-40b4-8a64-bfd4693388ac)
- [FDA Inspection 821840 - 2013-03-19](https://www.keypedia.com/records/fda_inspections/spentech-inc/6082bf67-9d59-4a82-94a1-4091b508a8b5)

Company: https://www.keypedia.com/companies/spentech-inc/720f7c67-477b-4f8d-b8cc-ba3b46c1104c

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