FDA Inspection
Midmark CorporationMidmark Corporation – FDA Inspection, Feb 24, 2010
Record Details
This FDA Inspection record concerns Midmark Corporation, with an inspection on February 24, 2010, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Midmark Corporation
- Inspection Date
- February 24, 2010
- Product Type
- Devices
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ID · cbdeaf2b-2ea4-4f90-9981-587009c39750
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 648559
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
FDA Citations
2- 21 CFR 803.50(a)(2)Individual Report of Malfunction
- 21 CFR 820.100(a)(3)Identification of actions needed
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Other FDA inspections of Midmark Corporation
3| Date | Classification | Office | Project area |
|---|---|---|---|
| March 14, 2024 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 22, 2017 | NAI | Center for Devices and Radiological Health | Radiation Control and Health Safety Act |
| March 13, 2012 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Midmark Corporation
- FDA Inspection 1234396 - 2024-03-14
- FDA Inspection 1026007 - 2017-08-22
- FDA Inspection 770816 - 2012-03-13
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