Quality Formulation Laboratories, Inc.

FDA inspection history in Paterson, New Jersey, 2009

1
Form 483

Every document, by year

  • Form 483

2009: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2009One Form 483, at Paterson, New Jersey.

Cited most

Across all Quality Formulation Laboratories observations on file

  • 21 CFR 111.15
    What sanitation requirements apply to your physical plant and grounds?
    15
  • 21 CFR 111.455
    What requirements apply to holding components, dietary supplements, packaging, and labels?
    3
  • 21 CFR 111.20
    What design and construction requirements apply to your physical plant?
    1
  • 21 CFR 111.27
    What requirements apply to the equipment and utensils that you use?
    1

The complete Quality Formulation Laboratories 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
2009-01-13483 Form 483$99

Investigators on these documents

Kerry A. Donovan (1)Valerie C. Reed (1)

FEI number 2243677 · most recent document Jan 13, 2009

About Quality Formulation Laboratories, Inc.

How many FDA Form 483s has Quality Formulation Laboratories, Inc. received?

FDA Intel has 1 Form 483 on file for Quality Formulation Laboratories, Inc.; the most recent is dated Jan 13, 2009.

When was Quality Formulation Laboratories, Inc. last inspected by FDA?

The most recent FDA inspection document on file for Quality Formulation Laboratories, Inc. is a Form 483 dated Jan 13, 2009, for the site in Paterson, New Jersey.

What did FDA cite at Quality Formulation Laboratories, Inc.?

The regulations cited most in the observations on file for Quality Formulation Laboratories, Inc. are 21 CFR 111.15 (What sanitation requirements apply to your physical plant and grounds?), 15 times; 21 CFR 111.455 (What requirements apply to holding components, dietary supplements, packaging, and labels?), 3 times; 21 CFR 111.20 (What design and construction requirements apply to your physical plant?), 1 time.