# FDA Inspection 960444 - Pharma Systems Eesti OU - February 19, 2016

Source: https://www.keypedia.com/records/fda_inspections/pharma-systems-eesti-ou/a80a3796-4384-4151-8c08-c1343c724186
Source feed: FDA_Inspections

> FDA Inspection 960444 for Pharma Systems Eesti OU on February 19, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 960444
- Company Name: Pharma Systems Eesti OU
- Inspection Date: 2016-02-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/pharma-systems-eesti-ou/ccd41dba-bfed-4559-bd70-9cba974976e0

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