FDA Inspection 1308330 — Thrombolex Inc

Thrombolex Inc — FEI 3015489145

The FDA completed an inspection of Thrombolex Inc on March 13, 2026 in New Britain, PA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 13, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
New Britain, PA (United States)