# Spentech, Inc. – FDA Inspection, Mar 19, 2013

Source: https://www.keypedia.com/records/fda_inspections/spentech-inc/6082bf67-9d59-4a82-94a1-4091b508a8b5
Source feed: FDA_Inspections

> FDA inspection 821840 of Spentech, Inc., March 19, 2013. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 821840
- Company Name: Spentech, Inc.
- Inspection Date: 2013-03-19
- 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: 1

## Related Documents

- [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/b4a8ef94-3b40-40b4-8a64-bfd4693388ac)
- [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

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