FDA Inspection 787354 — Mikrolab Stockholm AB

Mikrolab Stockholm AB — FEI 3002806287

The FDA completed an inspection of Mikrolab Stockholm AB on Jun 5, 2012 in Sollentuna. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 5, 2012
Fiscal Year
2012
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.