Home / Facilities / 1000125324

PureTek Corporation — FDA Facility Profile

FEI 1000125324

PureTek Corporation is an FDA-registered facility (FEI 1000125324) located in San Fernando, CA, US. Registered operations: ANALYSIS; LABEL; MANUFACTURE; PACK; RELABEL; REPACK. RegDataLab tracks 10 or more FDA inspections at this facility.

Facility Details

Location
San Fernando, CA (US)
Registration Expires
December 31, 2026
Operations
ANALYSIS; LABEL; MANUFACTURE; PACK; RELABEL; REPACK
Source
decrs

Recent inspections

  • 1262436 (VAI Fri Mar 07 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1116761 (VAI Thu Jan 30 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1034952 (VAI Fri Dec 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 949735 (VAI Tue Oct 27 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 919565 (VAI Wed Mar 18 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 860979 (VAI Wed Dec 18 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 808589 (NAI Tue Dec 04 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 734276 (NAI Wed Mar 16 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 707043 (NAI Fri Jan 21 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 675510 (VAI Fri Jul 16 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources