Rentschler Biopharma SE 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 1000291122.
Rentschler Biopharma SE
Laupheim, -, Germany
Issue DateDecember 06, 2016
FEI Number1000291122
CountryGermany
Status
No Warning LetterProduct Type
Drugs