# Global Flex Bed, Inc. – FDA Inspection, Jun 21, 2018

Source: https://www.keypedia.com/records/fda_inspections/global-flex-bed-inc/0e90d84c-c59f-4326-9544-12c9a267869b
Source feed: FDA_Inspections

> FDA inspection 1063752 of Global Flex Bed, Inc., June 21, 2018. Classification: Voluntary Action Indicated (VAI). Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1063752
- Company Name: Global Flex Bed, Inc.
- Inspection Date: 2018-06-21
- 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: 0

## Related Officers

- [Company Rep](https://www.keypedia.com/people/juanita-banuelos/b8b581ef-b9f3-4d77-a9fa-691223dbb7f4)

Company: https://www.keypedia.com/companies/global-flex-bed-inc/faef086a-9609-4d3f-9e61-c67657c540d3

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