# Clearstream Technologies Ltd – FDA Inspection, Jan 31, 2019

Source: https://www.keypedia.com/records/fda_inspections/clearstream-technologies-ltd/ed210896-c226-4257-9745-619b01348afe
Source feed: FDA_Inspections

> FDA inspection 1078231 of Clearstream Technologies Ltd, January 31, 2019. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1078231
- Company Name: Clearstream Technologies Ltd
- Inspection Date: 2019-01-31
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 4

## Related Documents

- FDA Inspection 1336196 - 2026-09-10
- FDA Inspection 968495 - 2016-04-21

## Related Officers

- [Company Rep](https://www.keypedia.com/people/maryam-tabatabaie/b792042d-e296-446d-90a9-d30c8f635506)

Company: https://www.keypedia.com/companies/clearstream-technologies-ltd/8ae8c7e0-89cc-4b7d-84c9-dca1798fea82

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