FDA Inspection
Midmark CorporationMidmark Corporation – FDA Inspection, Apr 2, 2018
Record Details
This FDA Inspection record concerns Midmark Corporation, with an inspection on April 2, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · fd6a54a6-e299-43aa-90e1-aefcb058ec11
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1048753
- FDA center
- Medical Devices & Rad Health
- Project area
- Postmarket Assurance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.100(a)Lack of or inadequate procedures
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Other FDA inspections of Midmark Corporation
5| Date | Classification | Office | Project area |
|---|---|---|---|
| August 15, 2019 | Not classified | Cincinnati District Office | |
| December 9, 2016 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 9, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 28, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 12, 2011 | OAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Midmark Corporation
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