FDA Inspection 1288372 — Exeltis Pharmaceuticals, Inc.

Exeltis Pharmaceuticals, Inc. — FEI 3036871012

The FDA completed an inspection of Exeltis Pharmaceuticals, Inc. on Jul 3, 2025 in Tekirdag. 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
Jul 3, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Tekirdag (Turkey)

Additional details

Bioanalytical BA/BE

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