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FDA Inspection 1181480 — Xymogen Manufacturing

Xymogen Manufacturing — FEI 3004315824

The FDA completed an inspection of Xymogen Manufacturing on August 8, 2022 in Orlando, FL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 8, 2022
Fiscal Year
2022
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Orlando, FL (United States)

Facility

Other inspections at this facility

  • 1246381 (VAI Tue Aug 13 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1062310 (VAI Thu Aug 16 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 897690 (VAI Wed Sep 10 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 833513 (OAI Fri May 24 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 790122 (VAI Fri Jul 06 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources