# FDA Inspection 572949 - Repligen Corporation - March 26, 2009

Source: https://www.keypedia.com/records/fda_inspections/repligen-corporation/9cd3c2f4-cfc1-49c6-9f64-3e7b59eaf731
Source feed: FDA_Inspections

> FDA Inspection 572949 for Repligen Corporation on March 26, 2009. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 572949
- Company Name: Repligen Corporation
- Inspection Date: 2009-03-26
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 853838 - 2013-11-04](https://www.keypedia.com/records/fda_inspections/repligen-corporation/abc58025-8cd9-4132-80df-c16e6334f2e2)
- [FDA Inspection 853838 - 2013-11-04](https://www.keypedia.com/records/fda_inspections/repligen-corporation/4d5436bb-0d54-4882-a7b2-e5604646de73)
- [FDA Inspection 843335 - 2013-08-07](https://www.keypedia.com/records/fda_inspections/repligen-corporation/bdc06bff-a18c-47cc-bbd0-929fde5bbf71)
- [FDA Inspection 572949 - 2009-03-26](https://www.keypedia.com/records/fda_inspections/repligen-corporation/1cc0b0be-2639-4f43-b9fc-5a46071d8791)

Company: https://www.keypedia.com/companies/repligen-corporation/398de28a-0906-41a5-a0bf-d8e8cd6a60f6

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