# FDA Inspection 930565 - Maxigen Biotech, Inc. - May 21, 2015

Source: https://www.keypedia.com/records/fda_inspections/maxigen-biotech-inc/62f856af-4332-4dd5-9a3b-cc5f2e8c21b7
Source feed: FDA_Inspections

> FDA Inspection 930565 for Maxigen Biotech, Inc. on May 21, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 930565
- Company Name: Maxigen Biotech, Inc.
- Inspection Date: 2015-05-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 617446 - 2009-10-01](https://www.keypedia.com/records/fda_inspections/maxigen-biotech-inc/84480214-0e5f-4de3-b39f-ab3b0886e631)

Company: https://www.keypedia.com/companies/maxigen-biotech-inc/82a7446d-3bfe-48d4-8b9b-a23ce614059a

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