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Entrotech Life Sciences, 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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Entrotech Life Sciences, Inc.

Columbus, Ohio, United States
Issue DateAugust 15, 2018
FEI Number3011393407
CountryUnited States
Status
No Warning Letter
Product Type
Devices
Entrotech Life Sciences, Inc. FDA Form 483, Columbus, Ohio, August 15, 2018