FDA Inspection 860131 — McNeil AB

McNeil AB — FEI 1000409186

The FDA completed an inspection of McNeil AB on December 13, 2013 in Helsingborg. 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
December 13, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Helsingborg (Sweden)