Cadila Pharmaceuticals Limited

FDA inspection history in Ankleshwar, India, 2014 to 2024

1
Form 483
1
Warning letter

Every document, by year

  • Form 483
  • Warning letter

2014: one warning letter; 2024: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2014One warning letter, at Ankleshwar, India.
  2. 2024One Form 483, at Ankleshwar, India.

Cited most

Across all Cadila Pharmaceuticals Limited observations on file

The complete Cadila Pharmaceuticals 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
2024-05-10483 Form 483$99
2014-10-15Warning letter Warning letter$99

Investigators on these documents

Alan A. Rivera (1)Angelica M. Hernandez (1)

FEI number 3002806711 · most recent document May 10, 2024

About Cadila Pharmaceuticals Limited

How many FDA Form 483s has Cadila Pharmaceuticals Limited received?

FDA Intel has 1 Form 483 on file for Cadila Pharmaceuticals Limited; the most recent is dated May 10, 2024.

When was Cadila Pharmaceuticals Limited last inspected by FDA?

The most recent FDA inspection document on file for Cadila Pharmaceuticals Limited is a Form 483 dated May 10, 2024, for the site in Ankleshwar, India.

What did FDA cite at Cadila Pharmaceuticals Limited?

The regulations cited most in the observations on file for Cadila Pharmaceuticals Limited are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.22 (Responsibilities of quality control unit), 1 time; 21 CFR 211.63 (Equipment design, size, and location), 1 time.

Has Cadila Pharmaceuticals Limited received an FDA warning letter?

Yes. FDA Intel has 1 FDA warning letter on file for Cadila Pharmaceuticals Limited; the most recent is dated Oct 15, 2014.