CERTIF'ICATE OF REGISTRATION This certifies thal: ROVIPHARM r.l;, 86 Route De Plan D Eau Treffort Val Revermont Auvergne, FRANCE F-01370 is registered with the U.S. Food and Drug Administration for FY 20l9-pursuant to Title 21, 8G:7 et seq. of the United...
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CERTIF'ICATE OF REGISTRATION This certifies thal: ROVIPHARM r.l;, 86 Route De Plan D Eau Treffort Val Revermont Auvergne, FRANCE F-01370 is registered with the U.S. Food and Drug Administration for FY 20l9-pursuant to Title 21, 8G:7 et seq. of the United States Code of Federal Regulations: Establishment Re gistration : 3005724348 , ;' Device Classification Name: DISPENSER, LIQUID MEDICATION Product Code: KYX Regulation Number: 880.6430 Official Correspondent Registrar Corp and U.S. Agent: 144 Research Drive, Hampton, Virginia, 23666,U51. Telephone: +I-7 57 -224-017 7' Fax: +l -7 57'224'017 9 Registrar Corp will con/irm that such registration remains ffictive upon request and presentation of this ceitificate untll the end of the year stated aboye, unless said registration is terminated after issuance of this certificate. Registrar Corp makes no other representations or warranties, nor does this certificate make any representationi o, ,arronties to any person or entity other than the nam
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