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ALS Czech Republic, S.R.O. 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.

To check this against FDA, open FDA's record for this establishment on FDA's Data Dashboard, which lists this inspection under FEI 3006712025.

ALS Czech Republic, S.R.O.

Prague 9, -, Czech Republic
Issue DateMay 29, 2018
FEI Number3006712025
CountryCzech Republic
Status
No Warning Letter
Product Type
Drugs
ALS Czech Republic, S.R.O. FDA Form 483, Prague 9, May 29, 2018