FDA Inspection
Honeywell Specialty Chemicals Seelze GmbHHoneywell Specialty Chemicals Seelze GmbH – FDA Inspection, Sep 15, 2017
Record Details
This FDA Inspection record concerns Honeywell Specialty Chemicals Seelze GmbH, with an inspection on September 15, 2017, issued by the Office of Inspections and Investigations, covering human drugs.
- Inspection Date
- September 15, 2017
- Product Type
- Human Drugs
View Company Profile
ID · 2012253c-b358-4bde-9620-ddbbe46aa3c2
Inspection Facts
- Inspection number
- 1032123
- FDA center
- Human Drugs
- Outcome
- Form 483 issued
Other FDA inspections of Honeywell Specialty Chemicals Seelze GmbH
2| Date | Classification | Office | Project area |
|---|---|---|---|
| April 19, 2024 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 19, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Honeywell Specialty Chemicals Seelze GmbH
- FDA Inspection 1236509 - 2024-04-19
- FDA Inspection 909933 - 2014-12-19
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