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Cambridge Heart, Inc. Form 483 Details

Form 483
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Source: FDA inspection recordConfirmed against FDA's published inspection data for this establishment and inspection date. FDA has published the inspection and what it cited, but not the form itself, which usually takes six to twelve months.

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Cambridge Heart, Inc.

Wilmington, Massachusetts, United States
Issue DateMarch 03, 2011
FEI Number3000215432
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Cambridge Heart, Inc. FDA Form 483, Wilmington, Massachusetts, March 3, 2011