Why FDA Inspection Conduct for API Plants

Why FDA inspection conduct for API plants | Key issues | Based on 5 Years trend Gaps in API Units

[@kiranyekula6302]

Very knowledgeable information sir tq

[@marepallisastry6419]

Explained very well sir

[@pakkiindu5162]

Hi sir very useful your videos

[@pakkiindu5162]

Enka videos pettandi sirrr

[@praveenchodapaneedi9512]

Difference between 21cfr and 483

[@vizagpharmasoluions]

21 CFR is guidelines (Code of Federal Register)
483 - It is form No. when FDA audit they raise any non conformity, they mention in FDA 483.