FDA Inspection
Arkema IncArkema Inc – FDA Inspection, Jun 7, 2018
Record Details
This FDA Inspection record concerns Arkema Inc, with an inspection on June 7, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.
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ID · 3126c67d-5464-4cec-a2fb-79c02a6fe65a
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1054865
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
FDA Citations
1- 21 CFR 211.194(a)(1)Sample identification and other information
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Other FDA inspections of Arkema Inc
6| Date | Classification | Office | Project area |
|---|---|---|---|
| August 14, 2026 | Not classified | New Orleans District Office | |
| May 25, 2023 | Not classified | New Orleans District Office | |
| January 26, 2016 | NAI | Center for Food Safety and Applied Nutrition | Pesticides and Chemical Contaminants |
| December 12, 2012 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 3, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Arkema Inc
- FDA Inspection 1330990 - 2026-08-14
- FDA Inspection 1206837 - 2023-05-25
- FDA Inspection 961398 - 2016-01-26
- FDA Inspection 810800 - 2012-12-12
- FDA Inspection 651005 - 2010-03-03
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