Greenwich Rx
Form 483 issued September 9, 2026 · Tomball, Texas
- Inspection
- Aug 17 – Sep 9, 2026
- Investigator
- Camerson E. Moore
- Observations
- 14
- Pages
- 11
- FEI number
- 3043120213
In short: On September 9, 2026, FDA issued a Form 483 with 14 observations to Greenwich Rx in Tomball, Texas (FEI 3043120213) after an inspection that ran Aug 17 – Sep 9, 2026. The investigator was Camerson E. Moore. Most observations concern production and facilities & equipment; the most-cited regulation is 21 CFR 211.113 (control of microbiological contamination).
At a glance
Production and facilities & equipment account for 12 of 14 observations.
Most cited: 21 CFR 211.113 (8×) · 211.42 (3×)
What FDA observed
Preview: the opening words of each observationDashed: section inferred by FDA Intel and checked against the regulation text
- 01
Use of ingredients not intended for phaimaceutical use…
- 02
Your firm produced drugs while construction was underway in an adjacent area without adequate controls to…
- 03
Microbial contamination was present in the ISO 5 area and areas…
- 04
Personnel were observed conducting aseptic manipulations where the movement of "first air" in the ISO 5…
This inspection in context
Camerson E. Moore
48 documents · 2014–2026
Cites 211.113 (control of microbiological contamination) more than any other section. Most of their documents are for sites in Texas.
The firmGreenwich Rx history
The site's inspection history, in date order.
Similar 483sOther sites cited under 211.113
See how FDA wrote the same problem up elsewhere.
Questions about this 483
What did FDA find at Greenwich Rx?
FDA listed 14 observations on this Form 483, mostly about production, facilities & equipment and materials. The most-cited regulation is 21 CFR 211.113 (control of microbiological contamination). The opening words of each observation are shown on this page.
Who inspected Greenwich Rx?
Camerson E. Moore is named on this Form 483, for the inspection of Aug 17 – Sep 9, 2026. Each investigator has a profile showing what they cite most.
When was Greenwich Rx inspected by FDA?
The inspection ran Aug 17 – Sep 9, 2026, and the Form 483 is dated September 9, 2026.
How do I get the full Form 483 for Greenwich Rx?
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.