FDA Inspection
Tarmac Products, Inc.Tarmac Products, Inc. – FDA Inspection, May 2, 2012
Record Details
This FDA Inspection record concerns Tarmac Products, Inc., with an inspection on May 2, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Tarmac Products, Inc.
- Inspection Date
- May 2, 2012
- Product Type
- Drugs
View Company Profile
ID · d66fc631-6203-42b1-ac46-5233141f0162
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 779095
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
7- 21 CFR 211.170(a)Active ingredient retained sample kept
- 21 CFR 211.100(b)Procedure Deviations Recorded and Justified
- 21 CFR 211.25(a)Training , Education , Experience overall
- 21 CFR 211.182Specific information required in individual logs
- 21 CFR 111.12(c)Personnel - education, training, experience
- 21 CFR 211.160(b)(4)Calibration - at intervals, written program, remedial action
- 21 CFR 111.25(a)Procedures - calibrating instruments
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Other FDA inspections of Tarmac Products, Inc.
9| Date | Classification | Office | Project area |
|---|---|---|---|
| February 6, 2026 | VAI | Florida District Office | Drug Quality Assurance |
| November 4, 2025 | VAI | Florida District Office | Compliance: Medical Devices |
| July 22, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 27, 2019 | OAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| November 10, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
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