# FDA Inspection 1008530 - Myelotec, Inc. - February 01, 2017

Source: https://www.globalkeysolutions.net/records/fda_inspections/myelotec-inc/460749d6-5c19-4740-8cdd-c83e31dcb2dd
Source feed: FDA_Inspections

> FDA Inspection 1008530 for Myelotec, Inc. on February 01, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1008530
- Company Name: Myelotec, Inc.
- Inspection Date: 2017-02-01
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 809094 - 2012-11-14](https://www.globalkeysolutions.net/records/fda_inspections/myelotec-inc/c61f40dc-f541-4698-acf2-1cfb87f5495f)
- [FDA Inspection 809094 - 2012-11-14](https://www.globalkeysolutions.net/records/fda_inspections/myelotec-inc/50fca8f5-eda7-4178-a93c-b408fcf3eac1)

Company: https://www.globalkeysolutions.net/companies/myelotec-inc/7e8b04cf-e54d-41f9-9e96-6e256646cb36

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