FDA Inspection 1270648 — TTY Biopharm Company Limited Lioudu Factory

TTY Biopharm Company Limited Lioudu Factory — FEI 3015497585

The FDA completed an inspection of TTY Biopharm Company Limited Lioudu Factory on April 22, 2025 in Keelung City. 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
April 22, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Keelung City (Taiwan)