Form 483

Rishi K. Wadhwa, M.D. Form 483, 2026-03-20

FDA issued a Form 483 to Rishi K. Wadhwa, M.D. on 2026-03-20 with 2 public-safe observations.

483· Form 483 issuedMedical Devices & Rad Health2 observations

Rishi K. Wadhwa, M.D. · Shreveport, United States · Issued March 20, 2026

Overview

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

Inspectional observations

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

20 Mar 2026
21 CFR 812.100

Investigator non-compliance with agreement/plan/regulations

Cited by Theressa B Smith

20 Mar 2026
21 CFR 812.140(a)(3)(ii)

Investigator records of relevant observations inadequate

Cited by Theressa B Smith

Inspected site

RKRishi K. Wadhwa, M.D.Shreveport, United States

Inspection team

Cited regulations

CFR citations associated with this Form 483.

CitationWhat it coversCited
21 CFR 812.100Cited across public-safe Form 483 observations1x
21 CFR 812.140(a)(3)(ii)Cited across public-safe Form 483 observations1x

Full 483 report

Get the verbatim text of all 2 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