FDA Inspection
Jane L. Rohlf, MDJane L. Rohlf, MD – FDA Inspection, Jul 19, 2016
Record Details
This FDA Inspection record concerns Jane L. Rohlf, MD, with an inspection on July 19, 2016, issued by the Center for Devices and Radiological Health, covering devices.
- Company
- Jane L. Rohlf, MD
- Inspection Date
- July 19, 2016
- Product Type
- Devices
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ID · 339ff2c0-ddb6-4ba2-a859-609714626f04
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 983479
- FDA center
- Medical Devices & Rad Health
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 812.100Investigator non-compliance with agreement/plan/regulations
- 21 CFR 812.140(a)(3)Investigator"s subject records inadequate
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Other FDA inspections of Jane L. Rohlf, MD
2| Date | Classification | Office | Project area |
|---|---|---|---|
| March 31, 2022 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| June 1, 2018 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for Jane L. Rohlf, MD
- FDA Inspection 1167083 - 2022-03-31
- FDA Inspection 1054870 - 2018-06-01
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