# Surmasis Pharmaceutical, LLC, Des Moines, IA – FDA Inspections

Source: https://www.keypedia.com/companies/surmasis-pharmaceutical-llc/6f9dfe3c-c8c3-4740-b9a8-0ecc1bb9b400

> Inspection records and compliance data for Surmasis Pharmaceutical, LLC in Des Moines, Iowa. 3 FDA inspections on record (1 OAI), 2 Form 483s, last inspected August 01, 2025.

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## Details

- Name: Surmasis Pharmaceutical, LLC
- FEI Number: 3011596846
- Business Operations: FDF MANUFACTURE, PACK
- Address Line 1: 4020 Gannett Ave
- City: Des Moines
- State: Iowa
- Zip Code: 50321
- Country Name: United States
- Address: 4020 Gannett Ave, Des Moines, Iowa 50321, United States
- Country: United States

## Related Documents

- [483 - Surmasis Pharmaceutical, LLC - 2025-08-01](https://www.keypedia.com/records/483/surmasis-pharmaceutical-llc/a9754776-fa7b-407d-9e77-3850f1791576) — source: FDA, date: August 1, 2025
- [FDA Inspection 1277270 - Surmasis Pharmaceutical, LLC - 2025-08-01](https://www.keypedia.com/records/fda_inspections/surmasis-pharmaceutical-llc/5fb29e39-e823-41b8-9d3c-db716adf874c) — classification: Voluntary Action Indicated (VAI), source: FDA, date: August 1, 2025
- [483 - Surmasis Pharmaceutical, LLC - 2020-03-19](https://www.keypedia.com/records/483/surmasis-pharmaceutical-llc/cefb989e-c11c-47e4-a8d6-fed612bc523b) — source: FDA, date: March 19, 2020
- FDA Inspection 1121169 - Surmasis Pharmaceutical, LLC - 2020-03-19 — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 19, 2020
- [EIR - Surmasis Pharmaceutical, LLC - 2018-03-01](https://www.keypedia.com/records/eir/surmasis-pharmaceutical-llc/0ba4c972-3f44-451c-9164-435274990ad9) — source: FDA, date: March 1, 2018
- [FDA Inspection 1042777 - Surmasis Pharmaceutical, LLC - 2018-03-01](https://www.keypedia.com/records/fda_inspections/surmasis-pharmaceutical-llc/e05262f6-17af-45f8-8849-59e1059d8573) — classification: Official Action Indicated (OAI), source: FDA, date: March 1, 2018
- FDA Inspection 1042777 - Surmasis Pharmaceutical, LLC - 2018-03-01 — classification: Official Action Indicated (OAI), source: FDA, date: March 1, 2018

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