# Flexion Therapeutics, Inc. – FDA Inspection, Jun 13, 2017

Source: https://www.keypedia.com/records/fda_inspections/flexion-therapeutics-inc/d57d79cc-b8b0-40ac-ba68-de65c43075e7
Source feed: FDA_Inspections

> FDA inspection 1013962 of Flexion Therapeutics, Inc., June 13, 2017. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1013962
- Company Name: Flexion Therapeutics, Inc.
- Inspection Date: 2017-06-13
- 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: 7

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/diane-m-biron/12eb885a-3ae3-449d-907e-36133dbdb194)
- [FDA Associated Person](https://www.keypedia.com/people/justine-m-corson/5f6e4477-f060-47f1-9165-a63fd6a36226)

Company: https://www.keypedia.com/companies/flexion-therapeutics-inc/fe3f8971-e741-4d3e-a390-5b4eda5df34e

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