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FDA Inspection 1013010 — Curia Massachusetts, Inc.

Curia Massachusetts, Inc. — FEI 3002951540

The FDA completed an inspection of Curia Massachusetts, Inc. on May 24, 2017 in Burlington, MA. 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
May 24, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Burlington, MA (United States)

Facility

Other inspections at this facility

  • 1210781 (NAI Thu Jun 29 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1134063 (NAI Wed Dec 02 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 988693 (VAI Wed Jul 13 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 877350 (NAI Fri May 02 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 841014 (VAI Thu Jul 18 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources