FDA Inspection
Nucro-Technics, Inc.Nucro-Technics, Inc. – FDA Inspection, Sep 11, 2013
Record Details
This FDA Inspection record concerns Nucro-Technics, Inc., with an inspection on September 11, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Nucro-Technics, Inc.
- Inspection Date
- September 11, 2013
- Product Type
- Drugs
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ID · 08f8a22d-02ea-492e-9473-57fc8921f6e0
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 849925
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
2- 21 CFR 211.25(a)GMP Training Frequency
- 21 CFR 211.160(b)(4)Written calibration procedures
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Other FDA inspections of Nucro-Technics, Inc.
5| Date | Classification | Office | Project area |
|---|---|---|---|
| May 20, 2025 | VAI | Office of Inspections and Investigations | Drug Quality Assurance |
| December 4, 2018 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 14, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 13, 2013 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 28, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Nucro-Technics, Inc.
- FDA Inspection 1271857 - 2025-05-20
- FDA Inspection 1073413 - 2018-12-04
- FDA Inspection 1001625 - 2016-12-14
- FDA Inspection 863723 - 2013-12-13
- FDA Inspection 648134 - 2010-01-28
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