FDA Investigator: Raphael Brykman
- Raphael Brykman first started conducting FDA inspections in 2011, with the last inspection in 2011. Over that time, Raphael Brykman has conducted 1 inspections at 1 companies across 1 sites.
Get Raphael Brykman's official FDA inspection documents. Gain valuable insights from their Form 483s and EIRs to ace your next inspection.
Documents
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FDA 483 Hi Tech Pharm Co., Ltd., Chungcheongbuk-Do | 2011
Out-of-stock
Raphael Brykman
Human Drug Form 483