# ERGO FLEX Technologies LLC – FDA Inspection, Apr 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/ergo-flex-technologies-llc/10531d1a-253c-4fe2-bbf5-b9bfcabe4dae
Source feed: FDA_Inspections

> FDA inspection 1022655 of ERGO FLEX Technologies LLC, April 10, 2017. Classification: Voluntary Action Indicated (VAI). 19 citations under 21 CFR parts 803 and 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1022655
- Company Name: ERGO FLEX Technologies LLC
- Inspection Date: 2017-04-10
- 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: 19

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/camerson-e-moore/50733244-0d55-4b0b-a758-f192b7c66457)

Company: https://www.keypedia.com/companies/ergo-flex-technologies-llc/529fedce-74dd-4ade-926d-b762a409b978

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