FDA Inspection 1080977 — Apotek Production & Laboratorier AB

Apotek Production & Laboratorier AB — FEI 3003766921

The FDA completed an inspection of Apotek Production & Laboratorier AB on December 13, 2018 in Umea. 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
December 13, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Umea (Sweden)