# FDA Inspection 826652 - Astute - April 15, 2013

Source: https://www.keypedia.com/records/fda_inspections/astute/c3a9d827-4b4d-49c0-b4d2-77c87a07f49d
Source feed: FDA_Inspections

> FDA Inspection 826652 for Astute on April 15, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 826652
- Company Name: Astute
- Inspection Date: 2013-04-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/astute/a68a6361-bed7-459b-91e1-2f24bb781570

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