# Cypress Medical Products LLC – FDA Inspection, May 8, 2018

Source: https://www.keypedia.com/records/fda_inspections/cypress-medical-products-llc/39a16bf4-3ca6-4ebf-80a8-162383bcb1e9
Source feed: FDA_Inspections

> FDA inspection 1051229 of Cypress Medical Products LLC, May 08, 2018. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1051229
- Company Name: Cypress Medical Products LLC
- Inspection Date: 2018-05-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 767155 - 2012-02-08](https://www.keypedia.com/records/fda_inspections/cypress-medical-products-llc/a23aaf26-20da-4512-9cc9-903ff02c5a5f)

## Related Officers

- [Tiki Dixon](https://www.keypedia.com/people/tiki-dixon/b3160a2c-ef16-4fa2-b9b9-4c3a0ed17c5b)

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

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