Inspection classificationInspection ended September 3, 2026
FDA inspection of Vios Fertility Institute St Louis DBA Kindbody of MO Medical Practice: NAI
No action indicated
FDA classified an inspection of Vios Fertility Institute St Louis DBA Kindbody of MO Medical Practice in Saint Louis, MO as NAI (no action indicated). The inspection ended on September 3, 2026. Product type: Biologics.
On the record
- Establishment
- Vios Fertility Institute St Louis DBA Kindbody of MO Medical Practice
- Location
- Saint Louis, MO
- Classification
- NAI · No action indicated
- Inspection ended
- 2026-09-03
- Product type
- Biologics
- Fiscal year
- FY2026
- FDA establishment identifier (FEI)
- 3021559133
- Source
- FDA Data Dashboard ↗
The full record
An account shows the project areas inspected and whether citations were posted.
What an inspection classification is
After an inspection FDA classifies the outcome. NAI (no action indicated): no objectionable conditions were found, or none that justify further action. VAI (voluntary action indicated): objectionable conditions were found, but the agency is not prepared to take or recommend regulatory action. OAI (official action indicated): regulatory or administrative action is recommended.
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