Colgate-Palmolive India Ltd.’
FDA inspection history in Mumbai, India, 2019
- 1
- Form 483
Every document, by year
- Form 483
2019: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2019One Form 483, at Mumbai, India.
Cited most
Across all Colgate-Palmolive India Ltd.’ observations on file
- 21 CFR 211.194(a)(4)Laboratory records1
- 21 CFR 211.22(d)Responsibilities of quality control unit1
The complete Colgate-Palmolive India Ltd.’ file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Mumbai, India
One Form 483 · 2019 · 2 observations
Latest: Form 483, May 3, 2019 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2019-05-03 | 483 Form 483 | Mumbai, India | 2 | $99 |
Investigators on these documents
FEI number 3004698222 · most recent document May 3, 2019
About Colgate-Palmolive India Ltd.’
How many FDA Form 483s has Colgate-Palmolive India Ltd.’ received?
FDA Intel has 1 Form 483 on file for Colgate-Palmolive India Ltd.’; the most recent is dated May 3, 2019.
When was Colgate-Palmolive India Ltd.’ last inspected by FDA?
The most recent FDA inspection document on file for Colgate-Palmolive India Ltd.’ is a Form 483 dated May 3, 2019, for the site in Mumbai, India.
What did FDA cite at Colgate-Palmolive India Ltd.’?
The regulations cited most in the observations on file for Colgate-Palmolive India Ltd.’ are 21 CFR 211.194(a)(4) (Laboratory records), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.