FDA Inspection
KBI Biopharma, Inc.KBI Biopharma, Inc. – FDA Inspection, Dec 9, 2016
Record Details
This FDA Inspection record concerns KBI Biopharma, Inc., with an inspection on December 9, 2016, issued by the Denver District Office, covering human drugs.
- Office
- Denver District Office
- People
- Marion Michaelis (Investigator)
- Monica M. Commerford (Issuing Officer)
View Company Profile
ID · ea62a328-0c07-423d-8103-b58f260812c3
Inspection Facts
- Inspection number
- 994318
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of KBI Biopharma, Inc.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| December 3, 2021 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 12, 2018 | Not classified | Denver District Office |
Other documents for KBI Biopharma, Inc.
- FDA Inspection 1158021 - 2021-12-03
- FDA Inspection 1066025 - 2018-09-12
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