FDA Inspection 1101587 — Nelipak Healthcare Packaging

Nelipak Healthcare Packaging — FEI 3012137049

The FDA completed an inspection of Nelipak Healthcare Packaging on August 21, 2019 in Phoenix, AZ. 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
August 21, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Phoenix, AZ (United States)