# FDA Inspection 995367 - GlasSpan Inc - November 09, 2016

Source: https://www.keypedia.com/records/fda_inspections/glasspan-inc/a3d9a6ef-650a-43ef-82c6-beb5fc0c7ed4
Source feed: FDA_Inspections

> FDA Inspection 995367 for GlasSpan Inc on November 09, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 995367
- Company Name: GlasSpan Inc
- Inspection Date: 2016-11-09
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 882684 - 2014-06-12](https://www.keypedia.com/records/fda_inspections/glasspan-inc/d435a2f5-0e74-434d-956f-ad579247c95a)
- [FDA Inspection 634786 - 2009-12-16](https://www.keypedia.com/records/fda_inspections/glasspan-inc/65ec02fa-1c69-44c8-a7e7-b8954256537d)
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Company: https://www.keypedia.com/companies/glasspan-inc/965bbf62-8cfc-4a8a-9bf0-10cddbdcd0d6

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