FDA Inspection 1117578 — Telix IsoTherapeutics Group, Inc.

Telix IsoTherapeutics Group, Inc. — FEI 3007294884

The FDA completed an inspection of Telix IsoTherapeutics Group, Inc. on February 3, 2020 in Angleton, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 3, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Angleton, TX (United States)