FDA Inspection 1232755 — Tulex Pharmaceuticals Inc.

Tulex Pharmaceuticals Inc. — FEI 3011875665

The FDA completed an inspection of Tulex Pharmaceuticals Inc. on Feb 29, 2024 in Cranbury, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Feb 29, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Cranbury, NJ (United States)

Additional details

Postmarket Adverse Drug Experience (PADE)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.