# FDA Inspection 908040 - Midbrook Inc. - December 22, 2014

Source: https://www.keypedia.com/records/fda_inspections/midbrook-inc/0a2f7c8f-0f61-4a55-8188-eccf4b59c0e2
Source feed: FDA_Inspections

> FDA Inspection 908040 for Midbrook Inc. on December 22, 2014. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 908040
- Company Name: Midbrook Inc.
- Inspection Date: 2014-12-22
- Classification: Official Action Indicated (OAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 908040 - 2014-12-22](https://www.keypedia.com/records/fda_inspections/midbrook-inc/a4ce423a-d99e-479f-93e2-1d4d8e52e3fe)
- [FDA Inspection 809894 - 2012-11-21](https://www.keypedia.com/records/fda_inspections/midbrook-inc/4fcdbbcc-7bdc-4d87-b1ff-1ce3ee06d3da)
- [FDA Inspection 809894 - 2012-11-21](https://www.keypedia.com/records/fda_inspections/midbrook-inc/f3606084-a6c2-4ad7-9510-10be7c0e5f12)

Company: https://www.keypedia.com/companies/midbrook-inc/b49734eb-f319-459f-b067-d04be12f2cc2

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