FDA Issues New Guidance on 21 CFR 211.11
The FDA has issued new guidance on “Considerations for Complying With 21 CFR 211.110.” According
Warning letters, 483s, Recalls, Import Alerts, Audit observations
The FDA has issued new guidance on “Considerations for Complying With 21 CFR 211.110.” According
Laurus, Visakh (India) was issued USFDA 483 with five (5) observations following USFDA inspection by
USFDA audit of Eugia US Manufacturing in New Jersey, US (FEI 3015534630) resulted in issuance