# CareFusion 303, Inc. - Inspection Records

Source: https://www.keypedia.com/companies/carefusion-303-inc/e44e5a89-d532-4564-ac5f-1aff2b7d8974

> Inspection records and compliance data for CareFusion 303, Inc. in San Diego, California. Access full analysis and detailed observations.

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## Details

- Name: CareFusion 303, Inc.
- FEI Number: 2016493
- City: San Diego
- State: California
- Country Name: United States
- Address Line 1: 10020 Pacific Mesa Blvd
- Zip Code: 92121
- Facility Type: Medical Device Manufacturer

## Related Documents

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- [FDA Inspection 1166360 - CareFusion 303, Inc. - 2022-03-10](https://www.keypedia.com/records/fda_inspections/carefusion-303-inc/f7c3363c-729a-4df5-8ff3-3d354a89d52f) — classification: No Action Indicated (NAI), source: FDA, date: March 10, 2022
- [483 - CareFusion 303, Inc. - 2020-04-06](https://www.keypedia.com/records/483/carefusion-303-inc/6fb77e5f-514f-4201-a4d9-a5cc5866ed99) — source: FDA, date: April 6, 2020
- [483 - CareFusion 303, Inc. - 2020-04-06](https://www.keypedia.com/records/483/carefusion-303-inc/f7ef7fac-ae70-4f01-8c52-6cfc2245a331) — source: FDA, date: April 6, 2020
- [FDA Inspection 1123377 - CareFusion 303, Inc. - 2020-04-06](https://www.keypedia.com/records/fda_inspections/carefusion-303-inc/1713d0c8-4785-4fa1-b345-8be4388f1500) — classification: Official Action Indicated (OAI), source: FDA, date: April 6, 2020
- [483 - CareFusion 303, Inc. - 2018-09-06](https://www.keypedia.com/records/483/carefusion-303-inc/2b146def-bcb7-4763-bebb-47a0f2ecc22d) — source: FDA, date: September 6, 2018
- [FDA Inspection 1064813 - CareFusion 303, Inc. - 2018-09-06](https://www.keypedia.com/records/fda_inspections/carefusion-303-inc/d8c98e27-b7c8-4d08-8036-9ec125168631) — classification: Official Action Indicated (OAI), source: FDA, date: September 6, 2018
- [FDA Inspection 1064813 - CareFusion 303, Inc. - 2018-09-06](https://www.keypedia.com/records/fda_inspections/carefusion-303-inc/21cd551f-a6f2-4cc8-8e02-e7aa779bcb8e) — classification: Official Action Indicated (OAI), source: FDA, date: September 6, 2018
- [FDA Inspection 987844 - CareFusion 303, Inc. - 2016-09-30](https://www.keypedia.com/records/fda_inspections/carefusion-303-inc/224b69cc-6441-4bed-b0cc-e7f798296ab6) — classification: No Action Indicated (NAI), source: FDA, date: September 30, 2016
- [FDA Inspection 987844 - CareFusion 303, Inc. - 2016-09-30](https://www.keypedia.com/records/fda_inspections/carefusion-303-inc/c92d27a0-655b-4bcc-99ca-d09edf38fba3) — classification: Official Action Indicated (OAI), source: FDA, date: September 30, 2016
- [FDA Inspection 893045 - CareFusion 303, Inc. - 2014-09-29](https://www.keypedia.com/records/fda_inspections/carefusion-303-inc/539e1b0a-7298-44fb-882f-ee6bcfc3dd6f) — classification: Official Action Indicated (OAI), source: FDA, date: September 29, 2014
- [FDA Inspection 893045 - CareFusion 303, Inc. - 2014-09-29](https://www.keypedia.com/records/fda_inspections/carefusion-303-inc/7349c143-674f-43ca-8951-4ab31502483c) — classification: Official Action Indicated (OAI), source: FDA, date: September 29, 2014
- [FDA Inspection 812020 - CareFusion 303, Inc. - 2012-12-18](https://www.keypedia.com/records/fda_inspections/carefusion-303-inc/49b88cc2-2c1c-4245-86a2-42935cc5c2be) — classification: No Action Indicated (NAI), source: FDA, date: December 18, 2012

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