# FDA Inspection 968362 - Octex Holdings, LLC. - April 20, 2016

Source: https://www.keypedia.com/records/fda_inspections/octex-holdings-llc/f31d6be5-2a9e-484d-8d86-ed27750bd2af
Source feed: FDA_Inspections

> FDA Inspection 968362 for Octex Holdings, LLC. on April 20, 2016. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 968362
- Company Name: Octex Holdings, LLC.
- Inspection Date: 2016-04-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1217145 - 2023-08-22](https://www.keypedia.com/records/fda_inspections/octex-holdings-llc/aaa6485b-e62c-4150-8f71-10652ef35b2b)
- [FDA Inspection 968362 - 2016-04-20](https://www.keypedia.com/records/fda_inspections/octex-holdings-llc/e1148b21-279e-4d7a-a3d3-483067805352)

Company: https://www.keypedia.com/companies/octex-holdings-llc/ff52d597-734c-43d5-b47f-7f180b660ad4

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