Molecular PharmaGroup LLC

FDA inspection history in New Providence, New Jersey, 2025 to 2026

1
Untitled letter
1
Form 483

Every document, by year

  • Untitled letter
  • Form 483

2025: one Form 483; 2026: one untitled letter.

The story so far

Built from the dates and citations on the documents themselves.

  1. 2025–26One Form 483 and one untitled letter, at New Providence, New Jersey.

Cited most

Across all Molecular PharmaGroup observations on file

The complete Molecular PharmaGroup 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
2026-02-05Untitled letter Untitled letter$99
2025-08-11483 Form 483$99

FEI number 3014413265 · most recent document Feb 5, 2026

About Molecular PharmaGroup LLC

How many FDA Form 483s has Molecular PharmaGroup LLC received?

FDA Intel has 1 Form 483 on file for Molecular PharmaGroup LLC; the most recent is dated Aug 11, 2025.

When was Molecular PharmaGroup LLC last inspected by FDA?

The most recent FDA inspection document on file for Molecular PharmaGroup LLC is a Form 483 dated Aug 11, 2025, for the site in New Providence, New Jersey.

What did FDA cite at Molecular PharmaGroup LLC?

The regulations cited most in the observations on file for Molecular PharmaGroup LLC are 21 CFR 211.113(b) (Control of microbiological contamination), 1 time; 21 CFR 211.180(e)(1) (General requirements), 1 time; 21 CFR 211.42(c)(10)(vi) (Design and construction features), 1 time.

Has Molecular PharmaGroup LLC received an FDA untitled letter?

Yes. FDA Intel has 1 FDA untitled letter on file for Molecular PharmaGroup LLC; the most recent is dated Feb 5, 2026. An untitled letter is FDA's enforcement letter for violations that don't rise to warning-letter level.