FDA Inspection 947080 — Apotek Produktion & Laboratorier AB

Apotek Produktion & Laboratorier AB — FEI 3002806290

The FDA completed an inspection of Apotek Produktion & Laboratorier AB on Oct 9, 2015 in Malmo. 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
Oct 9, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Malmo (Sweden)

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