FDA Inspection
OXFORD IMMUNOTEC INC DBA IMUGENOXFORD IMMUNOTEC INC DBA IMUGEN – FDA Inspection, Sep 15, 2017
Record Details
This FDA Inspection record concerns OXFORD IMMUNOTEC INC DBA IMUGEN, with an inspection on September 15, 2017, issued by the New England District Office, covering biologics.
- People
- Joyce A. Rockwell (Issuing Officer)
- Nicole M. Li (Issuing Officer)
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ID · d2f5f3a0-7af0-42cb-9aea-f88d53e2e55f
Inspection Facts
- Inspection number
- 1069500
- FDA center
- Biologics
- Outcome
- Form 483 issued
Other FDA inspections of OXFORD IMMUNOTEC INC DBA IMUGEN
2| Date | Classification | Office | Project area |
|---|---|---|---|
| August 16, 2013 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| July 21, 2011 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for OXFORD IMMUNOTEC INC DBA IMUGEN
- FDA Inspection 845914 - 2013-08-16
- FDA Inspection 735640 - 2011-07-21
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