Remendium Labs, LLC Form 483 Details
Form 483Source: 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.
To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3010771262.
Remendium Labs, LLC
Baton Rouge, Louisiana, United States
Issue DateAugust 03, 2016
FEI Number3010771262
CountryUnited States
Status
No Warning LetterProduct Type
Devices