FDA Inspection 965256 — TTY BioPharm Company Ltd (Chungli Factory)
The FDA completed an inspection of TTY BioPharm Company Ltd (Chungli Factory) on March 18, 2016 in Taoyuan. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- March 18, 2016
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Taoyuan (Taiwan)