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FDA Inspection 1060687 — Rechon Life Science AB

Rechon Life Science AB — FEI 3002806978

The FDA completed an inspection of Rechon Life Science AB on June 29, 2018 in Limhamn. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 29, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Limhamn (Sweden)

Facility

Other inspections at this facility

  • 1251480 (OAI Fri Sep 06 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1125627 (VAI Wed Nov 27 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 983550 (NAI Thu Jun 02 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 969057 (VAI Fri Apr 29 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 871626 (VAI Fri Mar 21 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources