Nephron Pharmaceuticals Corporation

FDA inspection history in West Columbia, South Carolina, 2017 to 2024

6
Form 483s

Every document, by year

  • Form 483

2017: one Form 483; 2018: one Form 483; 2019: one Form 483; 2022: one Form 483; 2023: one Form 483; 2024: one Form 483.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2017–19Three Form 483s, at West Columbia, South Carolina.
  2. 2022–24Three Form 483s, at West Columbia, South Carolina.
  3. 2023The longest 483 on file: 15 observations over 26 pages at West Columbia, South Carolina.

Cited most

Across all Nephron Pharmaceuticals observations on file

The complete Nephron Pharmaceuticals file.

All 6 documents as original PDFs, in one order. For supplier audits, diligence and inspection prep.

$505$594

15% off buying them one by one

Sites

Documents

6 on file, newest first
DateDocumentPrice
2024-09-25483 Form 483$99
2023-02-10483 Form 483$99
2022-04-20483 Form 483$99
2019-11-15483 Form 483$99
2018-04-20483 Form 483$99
2017-04-21483 Form 483$99

FEI number 3011158388 · most recent document Sep 25, 2024

About Nephron Pharmaceuticals Corporation

How many FDA Form 483s has Nephron Pharmaceuticals Corporation received?

FDA Intel has 6 Form 483s on file for Nephron Pharmaceuticals Corporation; the most recent is dated Sep 25, 2024.

When was Nephron Pharmaceuticals Corporation last inspected by FDA?

The most recent FDA inspection document on file for Nephron Pharmaceuticals Corporation is a Form 483 dated Sep 25, 2024, for the site in West Columbia, South Carolina.

What did FDA cite at Nephron Pharmaceuticals Corporation?

The regulations cited most in the observations on file for Nephron Pharmaceuticals Corporation are 21 CFR 211.42 (Design and construction features), 7 times; 21 CFR 211.113 (Control of microbiological contamination), 4 times; 21 CFR 211.160 (General requirements), 3 times.