# FDA Inspection 1226105 - Stericycle Inc - December 21, 2023

Source: https://www.keypedia.com/records/fda_inspections/stericycle-inc/48cd6462-247a-45eb-8fef-cd5ff821e4ef
Source feed: FDA_Inspections

> FDA Inspection 1226105 for Stericycle Inc on December 21, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1226105
- Company Name: Stericycle Inc
- Inspection Date: 2023-12-21
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1226105 - 2023-12-21](https://www.keypedia.com/records/fda_inspections/stericycle-inc/b15a3ccb-0034-4b55-ab67-a9ad94f8fda6)
- [FDA Inspection 1041855 - 2018-02-21](https://www.keypedia.com/records/fda_inspections/stericycle-inc/f861188e-c22e-418f-b0ef-e26d60771fdd)
- [FDA Inspection 1041855 - 2018-02-21](https://www.keypedia.com/records/fda_inspections/stericycle-inc/47a623f6-7ee0-4513-bbe4-c621f64cc701)

Company: https://www.keypedia.com/companies/stericycle-inc/a1207132-e501-4da5-961c-478ba7eafb54

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