FDA Inspection 1201271 — Sterizign Precision Technologies

Sterizign Precision Technologies — FEI 3014409963

The FDA completed an inspection of Sterizign Precision Technologies on March 16, 2023 in Brunswick, ME. 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 16, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Compliance: Devices
Location
Brunswick, ME (United States)