# FDA Inspection 1065812 - Myolyn Inc. - September 14, 2018

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

> FDA Inspection 1065812 for Myolyn Inc. on September 14, 2018. Classification: Voluntary Action Indicated (VAI).

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

## Related Documents

- [FDA Inspection 1065812 - 2018-09-14](https://www.globalkeysolutions.net/records/fda_inspections/myolyn-inc/6433d830-8798-45f5-b0ec-1ef3d4992fd0)

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

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