George Taub Products & Fusion Co,, Inc

FDA inspection history in Jersey City, New Jersey, 2024

1
Form 483

Every document, by year

  • Form 483

2024: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2024One Form 483, at Jersey City, New Jersey.

Cited most

Across all George Taub Products & Fusion Co observations on file

The complete George Taub Products & Fusion Co file.

All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.

$99

The documents one by one, while the file is prepared

See the documents

Sites

Documents

1 on file, newest first
DateDocumentPrice
2024-11-20483 Form 483$99

Investigators on these documents

Esteban Beltran (1)

FEI number 2241860 · most recent document Nov 20, 2024

About George Taub Products & Fusion Co,, Inc

How many FDA Form 483s has George Taub Products & Fusion Co,, Inc received?

FDA Intel has 1 Form 483 on file for George Taub Products & Fusion Co,, Inc; the most recent is dated Nov 20, 2024.

When was George Taub Products & Fusion Co,, Inc last inspected by FDA?

The most recent FDA inspection document on file for George Taub Products & Fusion Co,, Inc is a Form 483 dated Nov 20, 2024, for the site in Jersey City, New Jersey.

What did FDA cite at George Taub Products & Fusion Co,, Inc?

The regulations cited most in the observations on file for George Taub Products & Fusion Co,, Inc are 21 CFR 803.17 (What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), 1 time; 21 CFR 820.100(b) (Corrective and preventive action), 1 time; 21 CFR 820.181 (Device master record), 1 time.