FDA Inspection
Lonza AGLonza AG – FDA Inspection, Dec 15, 2017
Record Details
This FDA Inspection record concerns Lonza AG, with an inspection on December 15, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
- People
- Ashutosh V. Rao (Issuing Officer)
- Frances Namuswe (Issuing Officer)
- Maria J. Lopez- Barragan (Issuing Officer)
- Tiara N Brown-Crosen (Issuing Officer)
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ID · 6aabdbe9-cb78-4447-878b-509514b56a44
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1035618
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Lonza AG
11| Date | Classification | Office | Project area |
|---|---|---|---|
| October 28, 2025 | Not classified | Office of Inspections and Investigations | |
| April 4, 2025 | Not classified | Office of Inspections and Investigations | |
| March 28, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 21, 2019 | Not classified | Office of Inspections and Investigations | |
| March 29, 2019 | Not classified | Office of Inspections and Investigations |
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