# FDA Inspection 1031232 - AMYLIOR INC. - November 09, 2017

Source: https://www.keypedia.com/records/fda_inspections/amylior-inc/c41634e2-cc10-4fe6-9bb6-0978d9e081cb
Source feed: FDA_Inspections

> FDA Inspection 1031232 for AMYLIOR INC. on November 09, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031232
- Company Name: AMYLIOR INC.
- Inspection Date: 2017-11-09
- 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 1031232 - 2017-11-09](https://www.keypedia.com/records/fda_inspections/amylior-inc/f30d151e-3ee9-41a6-b2c5-5a00250950b2)

Company: https://www.keypedia.com/companies/amylior-inc/40deeb55-ea91-453e-8cb4-f2085d6e9e81

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