FDA Inspection 1129002 — Tulex Pharmaceuticals Inc.

Tulex Pharmaceuticals Inc. — FEI 3011875665

The FDA completed an inspection of Tulex Pharmaceuticals Inc. on August 14, 2020 in Cranbury, NJ. 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
August 14, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Cranbury, NJ (United States)