FDA Inspection 1228075 — Steripack Usa Limited Llc

Steripack Usa Limited Llc — FEI 3009656988

The FDA completed an inspection of Steripack Usa Limited Llc on January 11, 2024 in Lakeland, FL. 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
January 11, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Lakeland, FL (United States)