Compliance Program Guidance Manual Chapter – 42 Blood and Blood Products Inspection of Licensed In-Vitro Diagnostic (IVD) Devices 7342.008
Title:
Compliance Program Guidance Manual
Chapter – 42 Blood and Blood Products
Inspection of Licensed In-Vitro Diagnostic (IVD) Devices
7342.008
Origin/Publisher:
Freedom of Information Staff, (HFI 35), Food and Drug Administration, Rm. 12 A - 30, 5600 Fishers Lane, Rockville, MD 20857, USA, http://www.fda.gov/
Document Type:
Guidance Manual
Content:
Compliance Program CBER Biologics