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GovernmentDocs 5/4/2008 | 0 (0) | 41 | 0 | 0 | English
FDADocs 5/9/2008 | 0 (0) | 36 | 0 | 0 | English
FDADocs 5/9/2008 | 0 (0) | 26 | 0 | 0 | English
RMA 6/18/2008 | 0 (0) | 13 | 0 | 0 | English
July 12, 2001 SUBJECT: Commodity Hold and Recall ProcessAttached is the U.S. Department of...: ??? ??? ??? ??? ??? ??? ??? ??? institutionalizes USDA???s food recall/hold process; defines Federal, State ... more>>
farmservice 9/2/2008 | 0 (0) | 12 | 0 | 0 | English
MissPowerPoint 5/21/2008 | 0 (0) | 20 | 0 | 0 | English
Medicis Announces Voluntary Recall of Solodyn?? (minocycline HCL, USP) 90 Mg Tablets, Extended Release; Lot Numbers B080037 and B080038 Due to Product Mix-UpContact: Stericycle Customer Service ... more>>
GovernmentDocs 5/4/2008 | 0 (0) | 12 | 0 | 0 | English
Disetronic Medical Systems, Inc. July 13, 2006URGENT PRODUCT RECALLNotification of the New... Power Packs: Reference # BAT04697014001 and BAT3000813Issue Disetronic is conducting this recall of ... more>>
GovernmentDocs 5/4/2008 | 0 (0) | 16 | 0 | 0 | English
April 7, 2004 URGENT EXPANDED DRUG RECALL NOTIFICATION - PATIENT LEVEL Subject: DURAGESIC... Pharmacist: Janssen Pharmaceutica Products, L.P. would like to inform you of an expanded recall to users ... more>>
FDADocs 5/9/2008 | 0 (0) | 20 | 0 | 0 | English
URGENT: EXPANSION OF CLASS I PRODUCT RECALL AND PATIENT MANAGEMENT INFORMATION1Product Code: 0010202, Bard?? Composix?? Kugel Large Oval, 5.4??? x 7.0??? Product Code: 0010204, Bard?? Composix ... more>>
MissPowerPoint 6/20/2008 | 0 (0) | 5 | 0 | 0 | English
Stryker Trident Hip Implant Component Recall Latest Bad News for Company since FDA Warning Letter... Food & Drug Administration (FDA) warning letter about poor conditions at the Stryker plant in Mahwah ... more>>
FDADocs 5/9/2008 | 0 (0) | 15 | 0 | 0 | English
RECALL RETURN FAX Please check the appropriate box below, fill in the requested information, and return to us via fax or email ASAP so we can account for all vials of our compounded Colchicine. No ... more>>
FDADocs 5/9/2008 | 0 (0) | 16 | 0 | 0 | English
ProfessionalDocument 8/10/2008 | 0 (0) | 98 | 0 | 0 | English
Watson Announces Limited Recall of Fentanyl Transdermal System Watson Pharmaceuticals, Inc., a leading specialty pharmaceutical company, announced today that one lot of 75 mcg/hr Fentanyl Transdermal ... more>>
GovernmentDocs 5/4/2008 | 0 (0) | 163 | 2 | 0 | English
???FDA Regulatory Pathway???2nd Annual FDA and the Changing Paradigm for Tissue Regulation... Answers ??? ??? ??? ??? ??????361??? HCT/Ps??? No pre-market review--no application to FDA is ... more>>
FDADocs 5/9/2008 | 0 (0) | 132 | 0 | 0 | English
EXAMPLE United States Food and Drug Administration Los Angeles District Office1Notice of FDA ActionEntry Number: 112-9861457-6Notice Number: 2 November 6, 1996Filer: FBN Freight ... more>>
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