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FDA Inspection
•Instylla Inc•August 27, 2026

Instylla Inc – FDA Inspection, Aug 27, 2026

Record Details

This FDA Inspection record concerns Instylla Inc, with an inspection on August 27, 2026, issued by the New England District Office, covering medical devices & rad health.

Company
Instylla Inc
Inspection Date
August 27, 2026
Product Type
Medical Devices & Rad Health
Office
New England District Office
Person
  • Meredith L. Miller
View Company Profile

ID · fb50cd91-6174-495c-9acc-885f1941ed92

Inspection Facts

Inspection number
1333158
FDA center
Medical Devices & Rad Health
Project area
Project Evaluation: Devices
Outcome
Form 483 issued

FDA Citations

1
  1. 21 CFR 812.140(b)(5)Sponsor records of adverse device effects & complaints

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Instylla Inc

2
DateClassificationOfficeProject area
June 6, 2025NAICompliance: Devices
November 16, 2022NAICenter for Devices and Radiological HealthCompliance: Devices
Other documents for Instylla Inc
  • FDA Inspection 1272430 - 2025-06-06
  • FDA Inspection 1192016 - 2022-11-16

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