FDA Inspection 1040308 — STERIPACK MEDICAL POLAND SP. Z O. O.

STERIPACK MEDICAL POLAND SP. Z O. O. — FEI 3007766601

The FDA completed an inspection of STERIPACK MEDICAL POLAND SP. Z O. O. on Aug 30, 2017 in Jelcz-Laskowice. 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
Aug 30, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Project Evaluation: Devices
Location
Jelcz-Laskowice (Poland)

Additional details

Postmarket Audit Inspections

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