# AMYLIOR INC. – FDA Inspection, Nov 9, 2017

Source: https://www.keypedia.com/records/fda_inspections/amylior-inc/f30d151e-3ee9-41a6-b2c5-5a00250950b2
Source feed: FDA_Inspections

> FDA inspection 1031232 of AMYLIOR INC., November 09, 2017. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. Form 483 issued.

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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)
- 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: 6

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/laureen-m-geniusz/759a858e-e3f3-4c48-8194-9804c7ab2a7b)

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