FDA Inspection
Elixir CorporationElixir Corporation – FDA Inspection, Jan 10, 2018
Record Details
This FDA Inspection record concerns Elixir Corporation, with an inspection on January 10, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · e098c99c-d778-471d-8dc3-f74f1ab4eb31
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1039236
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Elixir Corporation
1| Date | Classification | Office | Project area |
|---|---|---|---|
| September 15, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Elixir Corporation
- FDA Inspection 988220 - 2016-09-15
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