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FDA Inspection
•Michael Todd Beauty LP•May 20, 2026

Michael Todd Beauty LP – FDA Inspection, May 20, 2026

Record Details

This FDA Inspection record concerns Michael Todd Beauty LP, with an inspection on May 20, 2026, issued by the Center for Devices and Radiological Health, covering medical devices & rad health.

Company
Michael Todd Beauty LP
Inspection Date
May 20, 2026
Product Type
Medical Devices & Rad Health
Office
Center for Devices and Radiological Health
Person
  • Alex J. Wild (Issuing Officer)
View Company Profile

ID · f214e4f0-58f3-46aa-a9b5-d180ad478a46

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1319206
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

FDA Citations

3
  1. 21 CFR 801.20(a)Label to bear a unique device identifier
  2. ISO 13485:2016 Clause 8.5.2Internal audit procedures not documented
  3. ISO 13485:2016 Clause 8.2.4Internal audit procedures not documented

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Michael Todd Beauty LP

2
DateClassificationOfficeProject area
July 25, 2023NAICenter for Devices and Radiological HealthCompliance: Devices
December 28, 2016NAICenter for Food Safety and Applied NutritionColors and Cosmetics Technology
Other documents for Michael Todd Beauty LP
  • FDA Inspection 1211109 - 2023-07-25
  • FDA Inspection 1003258 - 2016-12-28

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