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FDA Inspection 673832 — Octapharma Plasma, Inc.

Octapharma Plasma, Inc. — FEI 1071676

The FDA completed an inspection of Octapharma Plasma, Inc. on June 22, 2010 in Charlotte, NC. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
June 22, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Charlotte, NC (United States)

Facility

Other inspections at this facility

  • 1170457 (NAI Thu May 12 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1114211 (NAI Thu Oct 24 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1041438 (NAI Thu Jan 11 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 890539 (VAI Wed Aug 06 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 761649 (VAI Tue Dec 13 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources