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FDA Warning Letter — Philips Medical Systems (Cleveland) Inc

Case 158993 — FEI 1525965

The FDA took a Warning Letter action against Philips Medical Systems (Cleveland) Inc on June 7, 2011 (Cleveland, OH). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Philips Medical Systems (Cleveland) Inc
Date
June 7, 2011
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Cleveland, OH (United States)

Facility

Recent inspections

  • 1111084 (NAI Tue Nov 26 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1091789 (VAI Tue Jun 04 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1072883 (VAI Wed Oct 24 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1022578 (OAI Fri Aug 18 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 854978 (NAI Tue Jan 28 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources