FDA Inspection 1063000 — ALS Group USA, Corp.

ALS Group USA, Corp. — FEI 3005630502

The FDA completed an inspection of ALS Group USA, Corp. on Aug 20, 2018 in Phoenix, AZ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Aug 20, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Phoenix, AZ (United States)

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