FDA Inspection 1080880 — ALK-Abello, Inc.

ALK-Abello, Inc. — FEI 3006900385

The FDA completed an inspection of ALK-Abello, Inc. on Mar 1, 2019 in Plainville, CT. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Mar 1, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Plainville, CT (United States)