FDA Inspection 976058 — PolyPeptide Laboratories (Sweden) AB

PolyPeptide Laboratories (Sweden) AB — FEI 3002807004

The FDA completed an inspection of PolyPeptide Laboratories (Sweden) AB on May 27, 2016 in Limhamn. 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 27, 2016
Fiscal Year
2016
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.