FDA inspection
GERRESHEIMER PEACHTREE CITY LP: FDA inspection ending Mar 10, 2026
FDA inspection 1308758 · Official Action Indicated (OAI) · Peachtree City, Georgia
Key facts
| Inspection ID | 1308758 |
|---|---|
| Firm | GERRESHEIMER PEACHTREE CITY LP |
| FEI number | 3013445959 |
| Address | 650 Highway 74 S |
| City | Peachtree City |
| State | Georgia |
| ZIP | 30269 |
| Fiscal year | 2026 |
| Inspection end date | Mar 10, 2026 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Devices|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation|Compliance: Medical Devices|Generic Drug Evaluation |
| Product type | Devices, Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data