# FDA Inspection 599535 - Steris PLC - July 16, 2009

Source: https://www.globalkeysolutions.net/records/fda_inspections/steris-plc/c0710000-507e-420d-b03b-629b615809a3
Source feed: FDA_Inspections

> FDA Inspection 599535 for Steris PLC on July 16, 2009. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 599535
- Company Name: Steris PLC
- Inspection Date: 2009-07-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1223087 - 2023-11-06](https://www.globalkeysolutions.net/records/fda_inspections/steris-plc/be8a0958-950e-4a2c-97b4-074ab65e93be)
- [FDA Inspection 977303 - 2016-06-08](https://www.globalkeysolutions.net/records/fda_inspections/steris-plc/6fc73d70-bb30-4d89-bec6-0216be58c737)
- [FDA Inspection 915094 - 2015-02-27](https://www.globalkeysolutions.net/records/fda_inspections/steris-plc/4eaf1e20-ca98-4b2b-bbbc-33b4b663ef47)
- [FDA Inspection 915094 - 2015-02-27](https://www.globalkeysolutions.net/records/fda_inspections/steris-plc/91f51388-29c8-451c-8ea5-c25f47c52bba)
- [FDA Inspection 915094 - 2015-02-27](https://www.globalkeysolutions.net/records/fda_inspections/steris-plc/299fa52a-4517-44af-9787-99bf3f649eef)

Company: https://www.globalkeysolutions.net/companies/steris-plc/88ffc827-5fc2-41cd-b708-02b96911d97d

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