FDA Inspection 926966 — Mikrolab Stockholm AB

Mikrolab Stockholm AB — FEI 3002806287

The FDA completed an inspection of Mikrolab Stockholm AB on May 5, 2015 in Sollentuna. 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
May 5, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sollentuna (Sweden)

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