Shiseido America Inc.

FDA inspection history in East Windsor, New Jersey, 2018 to 2024

2
Form 483s

Every document, by year

  • Form 483

2018: one Form 483; 2024: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2018One Form 483, at East Windsor, New Jersey.
  2. 2018The longest 483 on file: 3 observations over 4 pages at East Windsor, New Jersey.
  3. 2024One Form 483, at East Windsor, New Jersey.

Cited most

Across all Shiseido America observations on file

The complete Shiseido America 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
2024-12-03483 Form 483$99
2018-11-01483 Form 483$99

Investigators on these documents

Ankur C. Patel (1)Nancy M. Espinal (1)

FEI number 3002653086 · most recent document Dec 3, 2024

About Shiseido America Inc.

How many FDA Form 483s has Shiseido America Inc. received?

FDA Intel has 2 Form 483s on file for Shiseido America Inc.; the most recent is dated Dec 3, 2024.

When was Shiseido America Inc. last inspected by FDA?

The most recent FDA inspection document on file for Shiseido America Inc. is a Form 483 dated Dec 3, 2024, for the site in East Windsor, New Jersey.

What did FDA cite at Shiseido America Inc.?

The regulations cited most in the observations on file for Shiseido America Inc. are 21 CFR 211.142(b) (Warehousing procedures), 1 time; 21 CFR 211.160(b) (General requirements), 1 time; 21 CFR 211.22(d) (Responsibilities of quality control unit), 1 time.