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FDA Inspection
•Tiller MIND BODY, Inc.•May 6, 2026

Tiller MIND BODY, Inc. – FDA Inspection, May 6, 2026

Record Details

This FDA Inspection record concerns Tiller MIND BODY, Inc., with an inspection on May 6, 2026, issued by the Center for Devices and Radiological Health, covering medical devices & rad health.

Company
Tiller MIND BODY, Inc.
Inspection Date
May 6, 2026
Product Type
Medical Devices & Rad Health
Office
Center for Devices and Radiological Health
Person
  • Katlin N. Stubbs
View Company Profile

ID · e2c4b0a4-5c14-40bd-8e1c-78c468e2b8b1

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1315762
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

FDA Citations

2
  1. ISO 13485:2016 Clause 7.5.1Production and service provision not adequate
  2. ISO 13485:2016 Clause 7.1Records of risk management activities in product realization not maintained

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Tiller MIND BODY, Inc.

3
DateClassificationOfficeProject area
July 13, 2023VAICenter for Devices and Radiological HealthCompliance: Devices
March 8, 2016NAICenter for Devices and Radiological HealthCompliance: Devices
June 26, 2014OAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Tiller MIND BODY, Inc.
  • FDA Inspection 1210048 - 2023-07-13
  • FDA Inspection 964024 - 2016-03-08
  • FDA Inspection 884539 - 2014-06-26

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