# FDA Inspection 839758 - Murex Biotech Ltd. - June 20, 2013

Source: https://www.keypedia.com/records/fda_inspections/murex-biotech-ltd/2ef761d8-49b0-4ecc-a079-d8751ebde80c
Source feed: FDA_Inspections

> FDA Inspection 839758 for Murex Biotech Ltd. on June 20, 2013. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 839758
- Company Name: Murex Biotech Ltd.
- Inspection Date: 2013-06-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 839758 - 2013-06-20](https://www.keypedia.com/records/fda_inspections/murex-biotech-ltd/6d761ba0-2649-4faa-8517-7128dfd1455c)
- [FDA Inspection 839758 - 2013-06-20](https://www.keypedia.com/records/fda_inspections/murex-biotech-ltd/cf71cf43-9124-40d0-9888-fe97cc0074ed)
- [FDA Inspection 804220 - 2012-06-28](https://www.keypedia.com/records/fda_inspections/murex-biotech-ltd/346df888-0b83-4bd6-8647-c2755a7b2789)

Company: https://www.keypedia.com/companies/murex-biotech-ltd/2f2a77d6-788e-4c74-892e-ce3b6ccca85f

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