# FDA Inspection 1220467 - Steri-Tek, LLC - September 26, 2023

Source: https://www.keypedia.com/records/fda_inspections/steri-tek-llc/5740ca0b-2caf-4306-8992-c00e74b88396
Source feed: FDA_Inspections

> FDA Inspection 1220467 for Steri-Tek, LLC on September 26, 2023. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1220467
- Company Name: Steri-Tek, LLC
- Inspection Date: 2023-09-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1234113 - 2024-03-26](https://www.keypedia.com/records/fda_inspections/steri-tek-llc/d921006f-0b18-4aca-a6e4-c0e79c8123b2)

Company: https://www.keypedia.com/companies/steri-tek-llc/c300ce41-306a-42d9-8c34-bed4c98866b6

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