FDA Inspection
TTY Biopham Company Ltd (Chung-Li Factory)TTY Biopham Company Ltd (Chung-Li Factory) – FDA Inspection, May 2, 2025
Record Details
This FDA Inspection record concerns TTY Biopham Company Ltd (Chung-Li Factory), with an inspection on May 2, 2025, issued by the Office of Inspections and Investigations, covering human drugs.
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ID · 92b1a8a4-7db4-4548-8a07-3fd267ed59da
Inspection Facts
- Inspection number
- 1271715
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of TTY Biopham Company Ltd (Chung-Li Factory)
3| Date | Classification | Office | Project area |
|---|---|---|---|
| November 16, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 18, 2016 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 27, 2013 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for TTY Biopham Company Ltd (Chung-Li Factory)
- FDA Inspection 1074092 - 2018-11-16
- FDA Inspection 965256 - 2016-03-18
- FDA Inspection 851466 - 2013-09-27
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