# FDA Inspection 632636 - Seecor, Inc - December 08, 2009

Source: https://www.keypedia.com/records/fda_inspections/seecor-inc/36c83866-bd8c-463a-ab1d-b85c6faa29ca
Source feed: FDA_Inspections

> FDA Inspection 632636 for Seecor, Inc on December 08, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 632636
- Company Name: Seecor, Inc
- Inspection Date: 2009-12-08
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 811430 - 2012-12-21](https://www.keypedia.com/records/fda_inspections/seecor-inc/0d406a66-f720-4dc3-aa9d-14863db4223d)
- [FDA Inspection 811430 - 2012-12-21](https://www.keypedia.com/records/fda_inspections/seecor-inc/c88f2818-a2e7-4f59-a2c0-bcc06a702d0a)
- [FDA Inspection 632636 - 2009-12-08](https://www.keypedia.com/records/fda_inspections/seecor-inc/08944d4a-6fe2-4fef-8b0e-9d9b1c9c6501)

Company: https://www.keypedia.com/companies/seecor-inc/27a582c6-3bf4-4cde-83eb-8a3fb3d299a7

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