# FDA Inspection 948473 - SureTek Medical - November 10, 2015

Source: https://www.keypedia.com/records/fda_inspections/suretek-medical/2a4a462c-2eec-4f5d-9eb6-b60087c9c35c
Source feed: FDA_Inspections

> FDA Inspection 948473 for SureTek Medical on November 10, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 948473
- Company Name: SureTek Medical
- Inspection Date: 2015-11-10
- 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/suretek-medical/f2d5fd3e-1b81-411b-82bc-2e32339f47ec

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