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FDA Inspection 919561 — Kedplasma LLC

Kedplasma LLC — FEI 2177765

The FDA completed an inspection of Kedplasma LLC on March 11, 2015 in Houston, TX. 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
March 11, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Houston, TX (United States)

Facility

Other inspections at this facility

  • 1195344 (NAI Tue Dec 06 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1010200 (NAI Tue Apr 18 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 831133 (NAI Thu Apr 25 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 742311 (NAI Wed Aug 03 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 603357 (VAI Tue Jul 21 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources