FDA Inspection 1228075 — Steripack Usa Limited Llc

Steripack Usa Limited Llc — FEI 3009656988

The FDA completed an inspection of Steripack Usa Limited Llc on Jan 11, 2024 in Lakeland, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jan 11, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Lakeland, FL (United States)

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