# FDA Inspection 767155 - Cypress Medical Products LLC - February 08, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/cypress-medical-products-llc/a23aaf26-20da-4512-9cc9-903ff02c5a5f
Source feed: FDA_Inspections

> FDA Inspection 767155 for Cypress Medical Products LLC on February 08, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 767155
- Company Name: Cypress Medical Products LLC
- Inspection Date: 2012-02-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1051229 - 2018-05-08](https://www.globalkeysolutions.net/records/fda_inspections/cypress-medical-products-llc/39a16bf4-3ca6-4ebf-80a8-162383bcb1e9)
- [FDA Inspection 767155 - 2012-02-08](https://www.globalkeysolutions.net/records/fda_inspections/cypress-medical-products-llc/8483d96b-5d02-4255-b6e2-931c5e46f742)

Company: https://www.globalkeysolutions.net/companies/cypress-medical-products-llc/eadd97f3-5e90-4e0c-808d-67780ee322dc

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