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FDA Inspection 982332 — LTS Lohmann Therapy Systems Corp

LTS Lohmann Therapy Systems Corp — FEI 1000121692

The FDA completed an inspection of LTS Lohmann Therapy Systems Corp on July 25, 2016 in West Caldwell, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 25, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
West Caldwell, NJ (United States)

Facility

Other inspections at this facility

  • 1231383 (NAI Thu Feb 01 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1092553 (VAI Tue Jun 11 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1039204 (NAI Thu Dec 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1017795 (VAI Thu Jul 13 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 949822 (NAI Mon Dec 07 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources