DR.REDDY'S Laboratories LIMITED

FDA inspection history across 2 sites, 2017 to 2024

5
Form 483s
1
EIR

Every document, by year

  • Form 483
  • EIR

2017: one inspection report; 2018: one Form 483; 2019: two Form 483s; 2021: one Form 483; 2024: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2017–21Four Form 483s and one inspection report, at Visakhapatnam, India and Duvvada, India.
  2. 2021The longest 483 on file: 8 observations over 18 pages at Duvvada, India.
  3. 2024One Form 483, at Visakhapatnam, India.

Cited most

Across all DR.REDDY'S Laboratories LIMITED observations on file

The complete DR.REDDY'S Laboratories LIMITED file.

All 6 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

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Sites

Also: one document not tied to a site.

Documents

6 on file, newest first
DateDocumentPrice
2024-05-17483 Form 483$99
2021-10-29483 Form 483$99
2019-08-20483 Form 483$99
2019-06-21483 Form 483$99
2018-10-30483 Form 483$99
2017-03-08EIR EIR$550

FEI number 3006549835 · most recent document May 17, 2024

About DR.REDDY'S Laboratories LIMITED

How many FDA Form 483s has DR.REDDY'S Laboratories LIMITED received?

FDA Intel has 5 Form 483s on file for DR.REDDY'S Laboratories LIMITED; the most recent is dated May 17, 2024.

When was DR.REDDY'S Laboratories LIMITED last inspected by FDA?

The most recent FDA inspection document on file for DR.REDDY'S Laboratories LIMITED is a Form 483 dated May 17, 2024, for the site in Visakhapatnam, India.

What did FDA cite at DR.REDDY'S Laboratories LIMITED?

The regulations cited most in the observations on file for DR.REDDY'S Laboratories LIMITED are 21 CFR 211.113 (Control of microbiological contamination), 3 times; 21 CFR 211.100 (Written procedures; deviations), 2 times; 21 CFR 211.160 (General requirements), 2 times.