FDA Inspection
Kathleen M. Mullane, D.O.Kathleen M. Mullane, D.O. – FDA Inspection, Feb 1, 2011
Record Details
This FDA Inspection record concerns Kathleen M. Mullane, D.O., with an inspection on February 1, 2011, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Kathleen M. Mullane, D.O.
- Inspection Date
- February 1, 2011
- Product Type
- Drugs
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ID · f7e6c472-a09b-4bee-af91-564663453573
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 713218
- FDA center
- Human Drugs
- Project area
- Bioresearch Monitoring
FDA Citations
3- 21 CFR 312.60FD-1572, protocol compliance
- 21 CFR 50.27(a)Consent form not approved/signed/dated
- 21 CFR 312.66Changes in research
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Other FDA inspections of Kathleen M. Mullane, D.O.
2| Date | Classification | Office | Project area |
|---|---|---|---|
| April 28, 2023 | NAI | Center for Biologics Evaluation and Research | Bioresearch Monitoring |
| July 20, 2020 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for Kathleen M. Mullane, D.O.
- FDA Inspection 1204393 - 2023-04-28
- FDA Inspection 1125458 - 2020-07-20
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