FDA Inspection
Curium US, LLCCurium US, LLC – FDA Inspection, Aug 18, 2023
Record Details
This FDA Inspection record concerns Curium US, LLC, with an inspection on August 18, 2023, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · a8baee89-fbb4-45fc-95a4-faf05caccce0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1216202
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Curium US, LLC
10| Date | Classification | Office | Project area |
|---|---|---|---|
| September 18, 2024 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| December 18, 2018 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| November 18, 2016 | Not classified | Kansas City District Office | |
| November 13, 2015 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| June 18, 2014 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Curium US, LLC
- FDA Inspection 1250722 - 2024-09-18
- FDA Inspection 1080170 - 2018-12-18
- FDA Inspection 996388 - 2016-11-18
- FDA Inspection 966441 - 2015-11-13
- FDA Inspection 884481 - 2014-06-18
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