FDA Inspection
Medi Manufacturing IncMedi Manufacturing Inc – FDA Inspection, Dec 21, 2016
Record Details
This FDA Inspection record concerns Medi Manufacturing Inc, with an inspection on December 21, 2016, issued by the Center for Devices and Radiological Health, covering devices.
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ID · 6a7e4c38-4b55-419e-90f9-c527fdafc459
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 996674
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 820.198(b)Review and evaluation for investigation
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Medi Manufacturing Inc
4| Date | Classification | Office | Project area |
|---|---|---|---|
| April 23, 2026 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 29, 2019 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| September 3, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 12, 2010 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Medi Manufacturing Inc
- FDA Inspection 1314370 - 2026-04-23
- FDA Inspection 1109936 - 2019-08-29
- FDA Inspection 846870 - 2013-09-03
- FDA Inspection 682463 - 2010-03-12
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