Colgate-Palmolive Company
FDA inspection history across 2 sites, 2014 to 2021
- 1
- Form 483
- 1
- Close-out
Every document, by year
- Form 483
- Close-out
2014: one close-out letter; 2021: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2014One close-out letter, at Piscataway, New Jersey.
- 2021One Form 483, at Morristown, Tennessee.
Cited most
Across all Colgate-Palmolive observations on file
- 21 CFR 803.18(b)(1)(i)What are the requirements for establishing and maintaining MDR files or records that apply to me?1
- 21 CFR 820.198(c)Complaint files1
- 21 CFR 820.72(a)Inspection, measuring, and test equipment1
- 21 CFR 820.75(b)Process validation1
The complete Colgate-Palmolive file.
All 2 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
Morristown, Tennessee
One Form 483 · 2021 · 4 observations
Latest: Form 483, Jul 15, 2021 →Piscataway, New Jersey
One close-out letter · 2014
Latest: Close-out, Aug 21, 2014 →
Documents
2 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2021-07-15 | 483 Form 483 | Morristown, Tennessee | 4 | $99 |
| 2014-08-21 | Close-out Close-out letter | Piscataway, New Jersey | — | $99 |
Investigators on these documents
FEI number 3005874880 · most recent document Jul 15, 2021
About Colgate-Palmolive Company
How many FDA Form 483s has Colgate-Palmolive Company received?
FDA Intel has 1 Form 483 on file for Colgate-Palmolive Company; the most recent is dated Jul 15, 2021.
When was Colgate-Palmolive Company last inspected by FDA?
The most recent FDA inspection document on file for Colgate-Palmolive Company is a Form 483 dated Jul 15, 2021, for the site in Morristown, Tennessee.
What did FDA cite at Colgate-Palmolive Company?
The regulations cited most in the observations on file for Colgate-Palmolive Company are 21 CFR 803.18(b)(1)(i) (What are the requirements for establishing and maintaining MDR files or records that apply to me?), 1 time; 21 CFR 820.198(c) (Complaint files), 1 time; 21 CFR 820.72(a) (Inspection, measuring, and test equipment), 1 time.