# Spentech, Inc. – FDA Inspection, Jul 27, 2017

Source: https://www.keypedia.com/records/fda_inspections/spentech-inc/d0bb5cbc-1b58-451b-bc41-e2e435c58ef5
Source feed: FDA_Inspections

> FDA inspection 1020883 of Spentech, Inc., July 27, 2017. Classification: No Action Indicated (NAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020883
- Company Name: Spentech, Inc.
- Inspection Date: 2017-07-27
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [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)
- [FDA Inspection 735761 - 2011-07-21](https://www.keypedia.com/records/fda_inspections/spentech-inc/5b54d5bc-1b06-4047-bd95-05aeb0fb899e)
- FDA Inspection 608313 - 2009-08-26

## Related Officers

- [Company Rep](https://www.keypedia.com/people/paul-m-kawamoto/0a24b110-12de-4736-8d98-7a023ceec01e)

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