# FDA Inspection 1078231 - Clearstream Technologies Ltd - January 31, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/clearstream-technologies-ltd/31ddd010-054b-4232-8a5b-ad6343774207
Source feed: FDA_Inspections

> FDA Inspection 1078231 for Clearstream Technologies Ltd on January 31, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1078231
- Company Name: Clearstream Technologies Ltd
- Inspection Date: 2019-01-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1078231 - 2019-01-31](https://www.globalkeysolutions.net/records/fda_inspections/clearstream-technologies-ltd/436616c0-6261-437f-99b4-fc96653ac55b)
- [FDA Inspection 1078231 - 2019-01-31](https://www.globalkeysolutions.net/records/fda_inspections/clearstream-technologies-ltd/ed210896-c226-4257-9745-619b01348afe)
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Company: https://www.globalkeysolutions.net/companies/clearstream-technologies-ltd/8ae8c7e0-89cc-4b7d-84c9-dca1798fea82

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