# FDA Inspection 808640 - Arrowhead DE LLC - November 20, 2012

Source: https://www.keypedia.com/records/fda_inspections/arrowhead-de-llc/45f96678-bfb3-4853-bfbb-9ce229329706
Source feed: FDA_Inspections

> FDA Inspection 808640 for Arrowhead DE LLC on November 20, 2012. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 808640
- Company Name: Arrowhead DE LLC
- Inspection Date: 2012-11-20
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1192732 - 2022-12-07](https://www.keypedia.com/records/fda_inspections/arrowhead-de-llc/b4198db8-b55c-4421-9c02-9b7e88b2fe8e)
- [FDA Inspection 1192732 - 2022-12-07](https://www.keypedia.com/records/fda_inspections/arrowhead-de-llc/454db7f3-2f46-4732-9cd0-9f27eb1555a5)
- [FDA Inspection 964562 - 2016-03-30](https://www.keypedia.com/records/fda_inspections/arrowhead-de-llc/a0690653-74e9-4881-b760-f0e7ace8c584)
- [FDA Inspection 768810 - 2012-02-21](https://www.keypedia.com/records/fda_inspections/arrowhead-de-llc/eb8aceb9-54bd-4be6-adc0-2be330fb9d20)

Company: https://www.keypedia.com/companies/arrowhead-de-llc/90ee4ec6-74ba-4ce1-a335-cbdec47ee50e

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