Revive Rx LLC dba Revive Rx Pharmacy

Form 483 issued March 27, 2026 · Houston, Texas

Inspection
Mar 9 – Mar 27, 2026
Observations
5
Pages
7
FEI number
3016710945

In short: On March 27, 2026, FDA issued a Form 483 with 5 observations to Revive Rx LLC dba Revive Rx Pharmacy in Houston, Texas (FEI 3016710945) after an inspection that ran Mar 9 – Mar 27, 2026. The investigator was Sangeeta M. Khurana. Most observations concern production; the most-cited regulation is 21 CFR 211.113 (control of microbiological contamination).

At a glance

5 of 5 observations on this 483 concern production.

Production5

Most cited: 21 CFR 211.113 (5×)

What FDA observed

Preview: the opening words of each observation

Dashed: section inferred by FDA Intel and checked against the regulation text

  1. 01

    Microbial contamination was present in the ISO 5 area and areas…

  2. 02

    Lack of adequate personnel…

  3. 03

    Smoke studies were not…

  4. 04

    Sterile drugs and Materials were expos ed to lower than…

1 more observation

Plus the full detail behind each one, exactly as FDA wrote it.

Get the full 483

This inspection in context

Questions about this 483

What did FDA find at Revive Rx LLC dba Revive Rx Pharmacy?

FDA listed 5 observations on this Form 483, mostly about production. 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 Revive Rx LLC dba Revive Rx Pharmacy?

Sangeeta M. Khurana is named on this Form 483, for the inspection of Mar 9 – Mar 27, 2026. Each investigator has a profile showing what they cite most.

When was Revive Rx LLC dba Revive Rx Pharmacy inspected by FDA?

The inspection ran Mar 9 – Mar 27, 2026, and the Form 483 is dated March 27, 2026.

How do I get the full Form 483 for Revive Rx LLC dba Revive Rx Pharmacy?

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.

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