# Diacor, Inc – FDA Inspection, Jun 19, 2013

Source: https://www.keypedia.com/records/fda_inspections/diacor-inc/ec5df3dc-96c9-4df3-a1e2-f6325281814b
Source feed: FDA_Inspections

> FDA inspection 836648 of Diacor, Inc, June 19, 2013. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 836648
- Company Name: Diacor, Inc
- Inspection Date: 2013-06-19
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1024795 - 2017-09-08](https://www.keypedia.com/records/fda_inspections/diacor-inc/b00ee590-6683-465b-aa92-c608f937809f)
- FDA Inspection 671010 - 2010-06-17
- [FDA Inspection 592352 - 2009-06-25](https://www.keypedia.com/records/fda_inspections/diacor-inc/669fbcfc-086b-4f2a-8481-9e8076b26e7f)

Company: https://www.keypedia.com/companies/diacor-inc/11688ab9-29f4-4edd-9d07-82c11bec238a

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