FDA Inspection
Howard Phillips LLC dba Phillips Co.Howard Phillips LLC dba Phillips Co. – FDA Inspection, Aug 11, 2016
Record Details
This FDA Inspection record concerns Howard Phillips LLC dba Phillips Co., with an inspection on August 11, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- August 11, 2016
- Product Type
- Drugs
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ID · 3d5df9f7-e3f3-47b6-9075-8e7cfa09a5e8
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 980708
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
4- 21 CFR 211.188Prepared for each batch, include complete information
- 21 CFR 211.196Distribution Record Requirements
- 21 CFR 211.186(a)Signature and checking of records -- 2 persons
- 21 CFR 211.22(a)Lack of quality control unit
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Other FDA inspections of Howard Phillips LLC dba Phillips Co.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| October 7, 2016 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 9, 2009 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Howard Phillips LLC dba Phillips Co.
- FDA Inspection 987780 - 2016-10-07
- FDA Inspection 588186 - 2009-06-09
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