A.P. Deauville, LLC

FDA inspection history across 2 sites, 2019 to 2025

2
Form 483s
1
Close-out

Every document, by year

  • Form 483
  • Close-out

2019: one close-out letter and one Form 483; 2025: one amended 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2019One close-out letter and one Form 483, at New Brunswick, New Jersey.
  2. 2019The longest 483 on file: 14 observations over 16 pages at New Brunswick, New Jersey.
  3. 2025One amended 483, at Easton, Pennsylvania.

Cited most

Across all A.P. Deauville observations on file

The complete A.P. Deauville file.

All 3 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$297

The price of the documents, added to your cart together

Sites

Documents

3 on file, newest first
DateDocumentPrice
2025-02-20Amended 483 Amended 483$99
2019-11-08Close-out Close-out letter$99
2019-05-02483 Form 483$99

Investigators on these documents

Adetutu Gidado (1)

FEI number 3004007943 · most recent document Feb 20, 2025

About A.P. Deauville, LLC

How many FDA Form 483s has A.P. Deauville, LLC received?

FDA Intel has 2 Form 483s on file for A.P. Deauville, LLC; the most recent is dated Feb 20, 2025.

When was A.P. Deauville, LLC last inspected by FDA?

The most recent FDA inspection document on file for A.P. Deauville, LLC is a Form 483 dated Feb 20, 2025, for the site in Easton, Pennsylvania.

What did FDA cite at A.P. Deauville, LLC?

The regulations cited most in the observations on file for A.P. Deauville, LLC are 21 CFR 211.103 (Calculation of yield), 2 times; 21 CFR 211.160(b) (General requirements), 2 times; 21 CFR 211.166 (Stability testing), 2 times.