FDA Inspection 854145 — PolyPeptide Laboratories (Sweden) AB

PolyPeptide Laboratories (Sweden) AB — FEI 3002807004

The FDA completed an inspection of PolyPeptide Laboratories (Sweden) AB on Sep 20, 2013 in Limhamn. 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
Sep 20, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Limhamn (Sweden)

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