Mankind Pharma Limited

FDA inspection history in Paonta Sahib, India, 2019 to 2022

2
Form 483s

Every document, by year

  • Form 483

2019: one Form 483; 2022: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2019One Form 483, at Paonta Sahib, India.
  2. 2022One Form 483, at Paonta Sahib, India.
  3. 2022The longest 483 on file: 6 observations over 18 pages at Paonta Sahib, India.

Cited most

Across all Mankind Pharma Limited observations on file

The complete Mankind Pharma Limited file.

All 2 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$198

The price of the documents, added to your cart together

Sites

Documents

2 on file, newest first
DateDocumentPrice
2022-02-25483 Form 483$99
2019-01-11483 Form 483$99

FEI number 3009083745 · most recent document Feb 25, 2022

About Mankind Pharma Limited

How many FDA Form 483s has Mankind Pharma Limited received?

FDA Intel has 2 Form 483s on file for Mankind Pharma Limited; the most recent is dated Feb 25, 2022.

When was Mankind Pharma Limited last inspected by FDA?

The most recent FDA inspection document on file for Mankind Pharma Limited is a Form 483 dated Feb 25, 2022, for the site in Paonta Sahib, India.

What did FDA cite at Mankind Pharma Limited?

The regulations cited most in the observations on file for Mankind Pharma Limited are 21 CFR 211.42 (Design and construction features), 2 times; 21 CFR 211.67 (Equipment cleaning and maintenance), 2 times; 21 CFR 211.192 (Production record review), 1 time.