# Arrowhead DE LLC – FDA Inspection, Feb 21, 2012

Source: https://www.keypedia.com/records/fda_inspections/arrowhead-de-llc/eb8aceb9-54bd-4be6-adc0-2be330fb9d20
Source feed: FDA_Inspections

> FDA inspection 768810 of Arrowhead DE LLC, February 21, 2012. Classification: Official Action Indicated (OAI). 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 768810
- Company Name: Arrowhead DE LLC
- Inspection Date: 2012-02-21
- Classification: Official Action Indicated (OAI)
- Classification Code: OAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 1322442 - 2026-06-17](https://www.keypedia.com/records/fda_inspections/arrowhead-de-llc/44ff7085-43eb-4a8b-9d23-119d3993a812)
- FDA Inspection 1192732 - 2022-12-07
- FDA Inspection 964562 - 2016-03-30
- FDA Inspection 808640 - 2012-11-20

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