# Midbrook Inc. – FDA Inspection, Dec 22, 2014

Source: https://www.keypedia.com/records/fda_inspections/midbrook-inc/a4ce423a-d99e-479f-93e2-1d4d8e52e3fe
Source feed: FDA_Inspections

> FDA inspection 908040 of Midbrook Inc., December 22, 2014. Classification: Official Action Indicated (OAI). 16 citations under 21 CFR parts 806 and 820. 1 other FDA inspection on record for this company.

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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)
- Classification Code: OAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 16

## Related Documents

- [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
