# Interscope, Inc. – FDA Inspection, Apr 22, 2019

Source: https://www.keypedia.com/records/fda_inspections/interscope-inc/c1cd2b94-2757-41b4-9043-0ceb66713c28
Source feed: FDA_Inspections

> FDA inspection 1087178 of Interscope, Inc., April 22, 2019. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1087178
- Company Name: Interscope, Inc.
- Inspection Date: 2019-04-22
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Documents

- [FDA Inspection 1205347 - 2023-05-05](https://www.keypedia.com/records/fda_inspections/interscope-inc/b880ee18-8e6f-4718-8420-3ddfcd36bd63)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/maryam-tabatabaie/b792042d-e296-446d-90a9-d30c8f635506)

Company: https://www.keypedia.com/companies/interscope-inc/bd9438fe-6dcd-4df7-ae00-4418482fc4c1

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7