FDA Inspection 604459 — ALK-Abello, Inc.

ALK-Abello, Inc. — FEI 3006900385

The FDA completed an inspection of ALK-Abello, Inc. on August 6, 2009 in Plainville, CT. 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
August 6, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Plainville, CT (United States)