# FDA Inspection 940519 - Halkey Roberts Corp - August 26, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/halkey-roberts-corp/8979378d-1881-46e2-9232-32cec7a839a6
Source feed: FDA_Inspections

> FDA Inspection 940519 for Halkey Roberts Corp on August 26, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 940519
- Company Name: Halkey Roberts Corp
- Inspection Date: 2015-08-26
- 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 940519 - 2015-08-26](https://www.globalkeysolutions.net/records/fda_inspections/halkey-roberts-corp/f2ef6e2d-d10b-45fe-a35b-a371fbd9ea60)
- [FDA Inspection 776758 - 2012-04-11](https://www.globalkeysolutions.net/records/fda_inspections/halkey-roberts-corp/c6d92cdc-f12c-461a-a9e6-d1450accdd4e)
- [FDA Inspection 776758 - 2012-04-11](https://www.globalkeysolutions.net/records/fda_inspections/halkey-roberts-corp/3262bfd5-c7ce-4ceb-b4e7-a8cac4539489)

Company: https://www.globalkeysolutions.net/companies/halkey-roberts-corp/c6382c98-2b4b-4e34-b73a-fa3fdb27ca3e

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