# FDA Inspection 998531 - Cardinal Health Ireland Manufacturing Limited - November 16, 2016

Source: https://www.keypedia.com/records/fda_inspections/cardinal-health-ireland-manufacturing-limited/8dee0e01-2276-41d4-8d42-4bf3f8d83724
Source feed: FDA_Inspections

> FDA Inspection 998531 for Cardinal Health Ireland Manufacturing Limited on November 16, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 998531
- Company Name: Cardinal Health Ireland Manufacturing Limited
- Inspection Date: 2016-11-16
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 753827 - 2011-10-27](https://www.keypedia.com/records/fda_inspections/cardinal-health-ireland-manufacturing-limited/7b737c01-e754-47c7-b188-482a2c9b4bf8)
- [FDA Inspection 563162 - 2009-01-29](https://www.keypedia.com/records/fda_inspections/cardinal-health-ireland-manufacturing-limited/b9afe94f-63fd-4eee-a6be-019a38459797)

Company: https://www.keypedia.com/companies/cardinal-health-ireland-manufacturing-limited/0948d2b8-2bca-4235-a670-347fa94556c8

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