FDA Inspection 1171682 — ALS Scandinavia AB

ALS Scandinavia AB — FEI 3007165135

The FDA completed an inspection of ALS Scandinavia AB on February 9, 2022 in Lulea. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 9, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lulea (Sweden)

Additional Details

Mutual Recognition Agreement (MRA)