# Myolyn Inc. – FDA Inspection, Sep 14, 2018

Source: https://www.keypedia.com/records/fda_inspections/myolyn-inc/70e82c54-010b-45cc-ace4-a1c5079ab24b
Source feed: FDA_Inspections

> FDA inspection 1065812 of Myolyn Inc., September 14, 2018. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1065812
- Company Name: Myolyn Inc.
- Inspection Date: 2018-09-14
- 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/richard-k-vogel/3ddd8bff-24fd-40ee-b0a7-fb5333a520f5)

Company: https://www.keypedia.com/companies/myolyn-inc/650b54fb-cd08-4448-9682-4afd1466b24d

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