FDA Inspection
Reese Pharmaceutical CompanyReese Pharmaceutical Company – FDA Inspection, Aug 4, 2009
Record Details
This FDA Inspection record concerns Reese Pharmaceutical Company, with an inspection on August 4, 2009, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Reese Pharmaceutical Company
- Inspection Date
- August 4, 2009
- Product Type
- Drugs
View Company Profile
ID · 3666ccbd-b259-4cde-bb55-252c8d06e915
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 602971
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
3- 21 CFR 211.170(b)Reserve samples identified, representative, stored
- 21 CFR 211.125(a)Strict control not exercised over labeling issued
- 21 CFR 211.100(b)SOPs not followed / documented
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Reese Pharmaceutical Company
7| Date | Classification | Office | Project area |
|---|---|---|---|
| September 25, 2025 | Not classified | Cincinnati District Office | |
| December 9, 2021 | NAI | Center for Food Safety and Applied Nutrition | Food Composition, Standards, Labeling and Econ |
| December 8, 2021 | NAI | Center for Food Safety and Applied Nutrition | Food Composition, Standards, Labeling and Econ |
| June 5, 2017 | NAI | Center for Food Safety and Applied Nutrition | Pesticides and Chemical Contaminants |
| April 25, 2017 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Reese Pharmaceutical Company
- FDA Inspection 1287906 - 2025-09-25
- FDA Inspection 1160702 - 2021-12-09
- FDA Inspection 1160701 - 2021-12-08
- FDA Inspection 1017672 - 2017-06-05
- FDA Inspection 1012578 - 2017-04-25
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