# FDA Inspection 1022655 - ERGO FLEX Technologies LLC - April 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 for ERGO FLEX Technologies LLC on April 10, 2017. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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