Form 483

Revive Rx LLC dba Revive Rx Pharmacy Form 483, 2026-03-27

FDA issued a Form 483 to Revive Rx LLC dba Revive Rx Pharmacy on 2026-03-27 with 5 public-safe observations.

483· Form 483 issuedHuman Drugs5 observations

Revive Rx LLC dba Revive Rx Pharmacy · Houston, United States · Issued March 27, 2026

Overview

  • 5 public-safe observations are available for this inspection.
  • 1 structured CFR citation is represented.
  • 1 investigator is tied to this Form 483.

Inspectional observations

Each observation cites the regulation FDA found the firm out of compliance with.

27 Mar 2026
FDCA 501(a)(2)(A)

Exposed to lower quality air/ISO 5

Cited by Sangeeta M Khurana

27 Mar 2026
FDCA 501(a)(2)(A)

Inadequate smoke studies

Cited by Sangeeta M Khurana

27 Mar 2026
FDCA 501(a)(2)(A)

Lack of, personnel sampling

Cited by Sangeeta M Khurana

27 Mar 2026
FDCA 501(a)(2)(A)

Lyophilizers, inadequately or not sterilized

Cited by Sangeeta M Khurana

27 Mar 2026
FDCA 501(a)(2)(A)

Microbial contamination was present, ISO 5/areas adjacent

Cited by Sangeeta M Khurana

Inspected site

RRRevive Rx LLC dba Revive Rx PharmacyHouston, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
FDCA 501(a)(2)(A)Cited across public-safe Form 483 observations5x

Full 483 report

Get the verbatim text of all 5 observations

The full inspection record, as Atlas holds it, so your team sees exactly what was cited and how it was answered.

  • The site's full inspection history around this Form 483
  • Whether these citations escalated to a warning letter
  • The investigators involved and the citations they repeat elsewhere