Neeyaan LLC
Form 483 issued January 27, 2026 · Cranbury, New Jersey
- Inspection
- Jan 13 – Jan 27, 2026
- Investigators
- Charlotte P. Chang· Janet A. Rajan
- Observations
- 25
- Pages
- 19
- FEI number
- 3024366553
In short: On January 27, 2026, FDA issued a Form 483 with 25 observations to Neeyaan LLC in Cranbury, New Jersey (FEI 3024366553) after an inspection that ran Jan 13 – Jan 27, 2026. The investigators were Charlotte P. Chang and Janet A. Rajan. Most observations concern dietary supplement CGMP and laboratory controls; the most-cited regulation is 21 CFR 111.70 (what specifications must you establish?).
At a glance
Observations span 4 systems, led by dietary supplement cgmp.
Most cited: 21 CFR 111.70 (4×) · 111.260 (2×)
What FDA observed
Preview: the opening words of each observationDashed: section inferred by FDA Intel and checked against the regulation text
- 01
Laboratory records are deficient in that they do not include a complete record of all…
- 02
There is no written testing program designed to assess the stability…
- 03
The accuracy, sensitivity, specificity, and reproducibility of test methods have not…
- 04
The responsibilities and procedures applicable to the quality control unit are not in…
This inspection in context
Charlotte P. Chang
3 documents · 2022–2026
Cites 111.70 (what specifications must you establish?) more than any other section. Most of their documents are for sites in New Jersey.
The firmNeeyaan LLC history
All 2 documents on file for this site, in date order, with what was cited at each inspection.
Similar 483sOther sites cited under 111.70
See how FDA wrote the same problem up elsewhere.
Questions about this 483
What did FDA find at Neeyaan LLC?
FDA listed 25 observations on this Form 483, mostly about dietary supplement CGMP, laboratory controls and production. The most-cited regulation is 21 CFR 111.70 (what specifications must you establish?). The opening words of each observation are shown on this page.
Who inspected Neeyaan LLC?
Charlotte P. Chang and Janet A. Rajan are named on this Form 483, for the inspection of Jan 13 – Jan 27, 2026. Each investigator has a profile showing what they cite most.
When was Neeyaan LLC inspected by FDA?
The inspection ran Jan 13 – Jan 27, 2026, and the Form 483 is dated January 27, 2026.
How do I get the full Form 483 for Neeyaan LLC?
Download the original PDF from FDA Intel for $99, with no subscription. Your first Form 483 or letter is on us. You also get an invoice PDF with the order.