Dabur India Limited
FDA inspection history across 2 sites, 2019 to 2026
- 2
- Form 483s
- 1
- Warning letter
Every document, by year
- Warning letter
- Form 483
2019: one Form 483; 2026: one warning letter and one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Silvassa, India.
- 2026One warning letter and one Form 483, at Dadra And Nagar Haveli, India.
- 2026The longest 483 on file: 7 observations over 9 pages at Dadra And Nagar Haveli, India.
Cited most
Across all Dabur India Limited observations on file
- 21 CFR 211.22(a)Responsibilities of quality control unit2
- 21 CFR 211.100(a)Written procedures; deviations1
- 21 CFR 211.180(e)(1)General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.56(a)Sanitation1
The complete Dabur India Limited file.
All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.
The price of the documents, added to your cart together
Sites
Dadra And Nagar Haveli, India
One Form 483 · 2026 · 7 observations
Latest: Form 483, Jan 16, 2026 →Silvassa, India
One Form 483 · 2019 · 2 observations
Latest: Form 483, Dec 6, 2019 →
Also: one document not tied to a site.
Documents
3 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-07-24 | Warning letter Warning letter | — | — | $99 |
| 2026-01-16 | 483 Form 483 | Dadra And Nagar Haveli, India | 7 | $99 |
| 2019-12-06 | 483 Form 483 | Silvassa, India | 2 | $99 |
Investigators on these documents
FEI number 3001413302 · most recent document Jul 24, 2026
About Dabur India Limited
How many FDA Form 483s has Dabur India Limited received?
FDA Intel has 2 Form 483s on file for Dabur India Limited; the most recent is dated Jan 16, 2026.
When was Dabur India Limited last inspected by FDA?
The most recent FDA inspection document on file for Dabur India Limited is a Form 483 dated Jan 16, 2026, for the site in Dadra And Nagar Haveli, India.
What did FDA cite at Dabur India Limited?
The regulations cited most in the observations on file for Dabur India Limited are 21 CFR 211.22(a) (Responsibilities of quality control unit), 2 times; 21 CFR 211.100(a) (Written procedures; deviations), 1 time; 21 CFR 211.180(e)(1) (General requirements), 1 time.
Has Dabur India Limited received an FDA warning letter?
Yes. FDA Intel has 1 FDA warning letter on file for Dabur India Limited; the most recent is dated Jul 24, 2026.