FDA Inspection 1273609 — Apotek Produktion & Laboratorier AB

Apotek Produktion & Laboratorier AB — FEI 3002806290

The FDA completed an inspection of Apotek Produktion & Laboratorier AB on Feb 29, 2024 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
Feb 29, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Malmo (Sweden)

Additional details

Mutual Recognition Agreement (MRA)

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