FDA Inspection
Repligen CorporationRepligen Corporation – FDA Inspection, Jan 25, 2018
Record Details
This FDA Inspection record concerns Repligen Corporation, with an inspection on January 25, 2018, issued by the Dallas District Office, covering medical devices & rad health.
- Company
- Repligen Corporation
- Inspection Date
- January 25, 2018
- Product Type
- Medical Devices & Rad Health
- Office
- Dallas District Office
View Company Profile
ID · 62248b2c-f737-4dbe-aa55-592fd0a24dd9
Inspection Facts
- Inspection number
- 1041140
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Repligen Corporation
4| Date | Classification | Office | Project area |
|---|---|---|---|
| February 8, 2024 | Not classified | Dallas District Office | |
| November 4, 2013 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| August 7, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| March 26, 2009 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Repligen Corporation
- FDA Inspection 1230139 - 2024-02-08
- FDA Inspection 853838 - 2013-11-04
- FDA Inspection 843335 - 2013-08-07
- FDA Inspection 572949 - 2009-03-26
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