FDA Inspection
Helixor Heilmittel GmbHHelixor Heilmittel GmbH – FDA Inspection, Jul 13, 2018
Record Details
This FDA Inspection record concerns Helixor Heilmittel GmbH, with an inspection on July 13, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · d438d10e-729b-4d7c-820f-777f05bef1fc
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1060828
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Helixor Heilmittel GmbH
1| Date | Classification | Office | Project area |
|---|---|---|---|
| September 12, 2025 | Not classified | Office of Inspections and Investigations |
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