FDA Inspection 1271746 — Steritec

Steritec — FEI 1000306139

The FDA completed an inspection of Steritec on June 3, 2025 in Athens, TX. 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
June 3, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Athens, TX (United States)