FDA Inspection
Neos Therapeutics, LPNeos Therapeutics, LP – FDA Inspection, Jul 25, 2017
Record Details
This FDA Inspection record concerns Neos Therapeutics, LP, with an inspection on July 25, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
- People
- Chunsheng Cai (Company Rep)
- Lisa R. Whitt (Issuing Officer)
View Company Profile
ID · 7f99fa2c-745e-4fdf-97f5-14bcf79149a8
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1021339
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
Other FDA inspections of Neos Therapeutics, LP
5| Date | Classification | Office | Project area |
|---|---|---|---|
| August 25, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 7, 2018 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 4, 2015 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 27, 2011 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 26, 2010 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Neos Therapeutics, LP
- FDA Inspection 1219358 - 2023-08-25
- FDA Inspection 1067923 - 2018-09-07
- FDA Inspection 929403 - 2015-06-04
- FDA Inspection 730235 - 2011-05-27
- FDA Inspection 648165 - 2010-02-26
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