# FDA Inspection 821449 - GE Parallel Design Inc - February 26, 2013

Source: https://www.keypedia.com/records/fda_inspections/ge-parallel-design-inc/a76f3e72-d918-4439-a6e9-477a04bb54dc
Source feed: FDA_Inspections

> FDA Inspection 821449 for GE Parallel Design Inc on February 26, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 821449
- Company Name: GE Parallel Design Inc
- Inspection Date: 2013-02-26
- 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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Company: https://www.keypedia.com/companies/ge-parallel-design-inc/6f95a985-d41c-4ebe-9ae1-a7a54932da56

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