FDA Inspection 1073636 — ALK-Abello, Inc.

ALK-Abello, Inc. — FEI 3006900385

The FDA completed an inspection of ALK-Abello, Inc. on November 29, 2018 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
November 29, 2018
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Plainville, CT (United States)

Additional Details

Sponsor, Contract Research Organization