# FDA Inspection 935803 - Aretech, LLC - July 17, 2015

Source: https://www.keypedia.com/records/fda_inspections/aretech-llc/ae032ba7-92b4-4b50-baf7-2be9c8d4fd3b
Source feed: FDA_Inspections

> FDA Inspection 935803 for Aretech, LLC on July 17, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 935803
- Company Name: Aretech, LLC
- Inspection Date: 2015-07-17
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 935803 - 2015-07-17](https://www.keypedia.com/records/fda_inspections/aretech-llc/5e51d380-f129-4f97-96fa-0fcfaa6656f6)

Company: https://www.keypedia.com/companies/aretech-llc/73c9d6e0-f595-45dd-b1f9-3d8efdc0b7d1

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