FDA Inspection
H. Michael MynattH. Michael Mynatt – FDA Inspection, Feb 7, 2013
Record Details
This FDA Inspection record concerns H. Michael Mynatt, with an inspection on February 7, 2013, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- H. Michael Mynatt
- Inspection Date
- February 7, 2013
- Product Type
- Devices
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ID · 40599763-6f66-4171-964d-fa9c9c7004c5
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 819965
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
1- 21 CFR 50.27(a)Consent form not approved/signed/dated
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