# Sentara Infusion Services, Chesapeake, VA – FDA Inspections

Source: https://www.keypedia.com/companies/sentara-infusion-services/96cac868-e9c3-442c-883e-d92b5ac0fd49

> Inspection records and compliance data for Sentara Infusion Services in Chesapeake, Virginia. 3 FDA inspections on record (2 OAI), 1 Form 483, last inspected December 16, 2022.

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## Details

- Name: Sentara Infusion Services
- FEI Number: 3011627411
- Facility Type: Producer of Sterile Drug Products
- Address Line 1: 535 Independence Pkwy Ste 300
- City: Chesapeake
- State: Virginia
- Zip Code: 23320
- Country Name: United States
- Address: 535 Independence Pkwy Ste 300, Chesapeake, Virginia 23320, United States
- Country: United States

## Related Documents

- [483 - Sentara Infusion Services - 2022-12-16](https://www.keypedia.com/records/483/sentara-infusion-services/b2b72b87-386a-414e-aa98-f8c8d65b2d85) — source: FDA, date: December 16, 2022
- [FDA Inspection 1193101 - Sentara Infusion Services - 2022-12-16](https://www.keypedia.com/records/fda_inspections/sentara-infusion-services/8c23963a-af93-4502-9951-7946cec0b8cb) — classification: Official Action Indicated (OAI), source: FDA, date: December 16, 2022
- [FDA Inspection 1064475 - Sentara Infusion Services - 2018-08-06](https://www.keypedia.com/records/fda_inspections/sentara-infusion-services/1244f8ac-1857-4dfd-997a-2527fcb9cc08) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 6, 2018
- [483_RESPONSE - Sentara Infusion Services - 2015-07-23](https://www.keypedia.com/records/483_response/sentara-infusion-services/b0494455-9d68-4099-bd6b-7bc57e1aaa4c) — source: FDA, date: July 23, 2015
- [483 - Sentara Infusion Services - 2015-07-23](https://www.keypedia.com/records/483/sentara-infusion-services/0478b531-fb04-4648-8c20-73afd0a0f657) — source: FDA, date: July 23, 2015
- [FDA Inspection 936197 - Sentara Infusion Services - 2015-07-23](https://www.keypedia.com/records/fda_inspections/sentara-infusion-services/42648017-9c24-41da-8ea8-ef5af02a5b2b) — classification: Official Action Indicated (OAI), source: FDA, date: July 23, 2015

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