FDA Inspection 860131 — McNeil AB

McNeil AB — FEI 1000409186

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.