FDA Inspection
Lonza Biologics, Inc.Lonza Biologics, Inc. – FDA Inspection, Aug 26, 2016
Record Details
This FDA Inspection record concerns Lonza Biologics, Inc., with an inspection on August 26, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Lonza Biologics, Inc.
- Inspection Date
- August 26, 2016
- Product Type
- Drugs
View Company Profile
ID · 59c02fcb-6426-4f57-9094-3a6566e4d6aa
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 988692
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Lonza Biologics, Inc.
12| Date | Classification | Office | Project area |
|---|---|---|---|
| April 16, 2026 | Not classified | New England District Office | Blood and Blood Products |
| February 6, 2026 | Not classified | New England District Office | |
| June 6, 2025 | Not classified | New England District Office | |
| July 12, 2024 | Not classified | New England District Office | |
| March 7, 2024 | NAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
Other documents for Lonza Biologics, Inc.
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