# FDA Inspection 835894 - Beckman Coulter Ireland, Inc. - May 01, 2013

Source: https://www.keypedia.com/records/fda_inspections/beckman-coulter-ireland-inc/8832c8cc-4411-4a3c-be91-da3aa5aa4289
Source feed: FDA_Inspections

> FDA Inspection 835894 for Beckman Coulter Ireland, Inc. on May 01, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 835894
- Company Name: Beckman Coulter Ireland, Inc.
- Inspection Date: 2013-05-01
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 835894 - 2013-05-01](https://www.keypedia.com/records/fda_inspections/beckman-coulter-ireland-inc/06639b6f-9d70-48eb-9e61-40f528a84e6f)
- [FDA Inspection 720057 - 2011-03-10](https://www.keypedia.com/records/fda_inspections/beckman-coulter-ireland-inc/efa0b725-66cd-4ca0-9e3c-3e5853a40f58)

Company: https://www.keypedia.com/companies/beckman-coulter-ireland-inc/adeacfc5-294c-4ef9-9775-1cf562214a0e

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