# FDA Inspection 648559 - Midmark  Corporation - February 24, 2010

Source: https://www.keypedia.com/records/fda_inspections/midmark-corporation/41fbb992-2d88-4ff9-a2d8-eaa629b8bc94
Source feed: FDA_Inspections

> FDA Inspection 648559 for Midmark  Corporation on February 24, 2010. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 648559
- Company Name: Midmark  Corporation
- Inspection Date: 2010-02-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1234396 - 2024-03-14](https://www.keypedia.com/records/fda_inspections/midmark-corporation/210b8f2a-1e88-49d0-b27b-f00d28aef9e2)
- [FDA Inspection 1026007 - 2017-08-22](https://www.keypedia.com/records/fda_inspections/midmark-corporation/4b9b6938-4b9f-456e-ac4f-83c5bba85dcb)
- [FDA Inspection 1026007 - 2017-08-22](https://www.keypedia.com/records/fda_inspections/midmark-corporation/8afa70e9-2922-4d54-a443-d765cf9acda0)
- [FDA Inspection 1026007 - 2017-08-22](https://www.keypedia.com/records/fda_inspections/midmark-corporation/851e9195-bb70-4de3-ac61-cb43503cd5a2)
- [FDA Inspection 770816 - 2012-03-13](https://www.keypedia.com/records/fda_inspections/midmark-corporation/f351ec07-071e-4e96-97c0-9c6ee51915ef)

Company: https://www.keypedia.com/companies/midmark-corporation/51d13b4b-8416-4e83-a405-672a2f2f543e

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