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FDA Warning Letter — Aesculap AG

Case 205233 — FEI 3002806315

The FDA took a Warning Letter action against Aesculap AG on September 26, 2011 (Tuttlingen, Germany). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Aesculap AG
Date
September 26, 2011
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Tuttlingen (Germany)

Facility

Recent inspections

  • 1178394 (NAI Thu Jul 21 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 987720 (NAI Thu Sep 22 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 939850 (NAI Thu Jul 16 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 841575 (NAI Thu Jul 04 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 809376 (NAI Tue Dec 04 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources