Horiba ABX SAS 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 3000148879.
Horiba ABX SAS
Montpellier, -, France
Issue DateJune 29, 2017
FEI Number3000148879
CountryFrance
Status
No Warning LetterProduct Type
Devices