# FDA Inspection 931144 - Digirad Corporation - June 18, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/digirad-corporation/e519abab-074b-4e2a-93c8-ea85d1936081
Source feed: FDA_Inspections

> FDA Inspection 931144 for Digirad Corporation on June 18, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 931144
- Company Name: Digirad Corporation
- Inspection Date: 2015-06-18
- 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.globalkeysolutions.net/companies/digirad-corporation/8c21578c-8aed-43b2-9434-6155a60291ef

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