# Accumedix, Inc. – FDA Inspection, Aug 19, 2010

Source: https://www.keypedia.com/records/fda_inspections/accumedix-inc/af2649dd-bf3a-4755-96b6-b7ba8cacf5b1
Source feed: FDA_Inspections

> FDA inspection 678206 of Accumedix, Inc., August 19, 2010. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 678206
- Company Name: Accumedix, Inc.
- Inspection Date: 2010-08-19
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 985551 - 2016-08-17
- FDA Inspection 846362 - 2013-08-06
- [FDA Inspection 756447 - 2011-12-05](https://www.keypedia.com/records/fda_inspections/accumedix-inc/8f8f22e4-e78e-4865-9b3a-6ac8fe682f58)

Company: https://www.keypedia.com/companies/accumedix-inc/0a54718e-efa8-403c-a68d-41b7dc2036e7

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